K162588 · Moller Medical GmbH · KNW · Jun 19, 2017 · Gastroenterology, Urology
Device Facts
Record ID
K162588
Device Name
Möller Medical Biopsy Needles and Systems
Applicant
Moller Medical GmbH
Product Code
KNW · Gastroenterology, Urology
Decision Date
Jun 19, 2017
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 876.1075
Device Class
Class 2
Indications for Use
The Möller Medical Biopsy Needles and Systems are used to obtain core samples and aspiration from tissue by biopsy. The various wall thicknesses, diameters, tip geometries and cutting techniques of the different hollow needle types and biopsy systems affect the quality of the biopsy specimen. Model BOW-1060 bone marrow biopsy systems are intended for the atraumatic taking of specimens from and inside bones. Application areas of the products are bone respectively bone marrow. Model BOW-1070 bone marrow aspiration biopsy set is intended for aspiration in the area of the sternum or lilac crest. Application areas of the products are bone respectively bone marrow. Model BOY-1080 bone biopsy needle set has been designed for atraumatic bone biopsy. Application areas of the products are bone respectively bone marrow. Model DNG-10XX single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions and are combined with biopsy guns. Model full-sCore® DNG-2020 disposable biopsy needles are intended only for biopsies on soft tissue and tissue from soft, internal organs such as liver, kidney, breast, lung and various soft tissue lesions , and should be used with the Möller Medical Blue (RBG-1000-10-1000) biopsy gun. Model FNB and MBY single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue for example from pleura cavity and associated organs, abdominal cavity and associated organs like breast, liver, prostate and kidnev. Model COX is for safe needle guidance and for taking several biopsy specimens. for example from liver, kidney, breast. thyroid, pancreas, spleen, lung and various soft tissue lesions, with only one single puncture. Model ABG disposable automatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions. Model SBG disposable semiautomatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions. Model Möller Medical Blue RBG is a reusable, automatic biopsy gun that is intended exclusively for use with DNG-1020 / full-sCore® DNG-2020 disposable needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions. When used for breast biopsy, the product is for diagnosis only. The extent of histological abnormality cannot be reliably determined from its mammographic appearance. Therefore, the extent of removal of the imaged evidence of an abnormality does not predict the extent of removal of a histological abnormality; e.g., malignancy. When the sampled abnormality is not histologically benign, it is essential that the tissue margins be examined for completeness of removal of using standard surgical procedures.
Device Story
Portfolio of biopsy instruments including manual needles, semi-automatic/automatic biopsy guns, and coaxial introducers; used for harvesting bone, bone marrow, and soft tissue core/aspiration samples. Operation: physician inserts needle/gun under imaging guidance (CT/Ultrasound); automatic/semi-automatic guns use spring-loaded mechanisms to advance stylet and cannula to capture tissue. Coaxial needles allow multiple biopsies via single puncture. Output: tissue specimen for histological/cytological analysis. Used in clinical settings by physicians. Benefits: enables minimally invasive tissue sampling for diagnostic evaluation.
Clinical Evidence
Bench testing only. Tests included intensity/preclearance, shelf life (5 years), artificial ageing, firing tests, pull-out force, and functionality (50 insertions). All tests passed predetermined criteria.
Technological Characteristics
Manual and spring-loaded biopsy instruments. Materials: medical-grade metals/plastics consistent with predicate devices. Features: various wall thicknesses, diameters, tip geometries, and cutting techniques. Connectivity: none. Sterilization: sterile (single-use) or reprocessable (reusable gun).
Indications for Use
Indicated for core biopsy and aspiration of bone, bone marrow, and soft tissues (liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung, pleura, abdominal cavity). For breast biopsy, diagnosis only; does not predict histological abnormality extent. Contraindications: none stated.
Regulatory Classification
Identification
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
{0}------------------------------------------------
Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized caduceus symbol, which is a staff with two snakes entwined around it. The logo is surrounded by the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement. The text is written in all capital letters.
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
June 19, 2017
Möller Medical GmbH Ms. Angela Kikowatz Regulatory Affairs Manager Wasserkuppenstrasse 29-31 Fulda, 36043 Germany
Re: K162588
Trade/Device Name: Möller Medical Biopsv Needles and Systems Regulation Number: 21 CFR 876.1075 Regulation Name: Gastroenterology-Urology-Biopsy Instrument Regulatory Class: Class II Product Code: KNW Dated: May 31, 2017 Received: June 5, 2017
Dear Ms. Kikowatz:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical devicerelated adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
{1}------------------------------------------------
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to
http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.
You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address
http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.
Sincerely, Jennifer R. Stevenson -S3 For Binita S. Ashar, M.D., M.B.A., F.A.C.S. Director
Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
## Indications for Use
510(k) Number (if known) K162588
## Device Name
Möller Medical Biopsy Needles and Systems
#### Indications for Use (Describe)
The Möller Medical Biopsy Needles and Systems are used to obtain core samples and aspiration from tissue by biopsy. The various wall thicknesses, diameters, tip geometries and cutting techniques of the different hollow needle types and biopsy systems affect the quality of the biopsy specimen.
Model BOW-1060 bone marrow biopsy systems are intended for the atraumatic taking of specimens from and inside bones. Application areas of the products are bone respectively bone marrow.
Model BOW-1070 bone marrow aspiration biopsy set is intended for aspiration in the area of the sternum or lilac crest. Application areas of the products are bone respectively bone marrow.
Model BOY-1080 bone biopsy needle set has been designed for atraumatic bone biopsy. Application areas of the products are bone respectively bone marrow.
Model DNG-10XX single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions and are combined with biopsy guns.
Model full-sCore® DNG-2020 disposable biopsy needles are intended only for biopsies on soft tissue and tissue from soft, internal organs such as liver, kidney, breast, lung and various soft tissue lesions , and should be used with the Möller Medical Blue (RBG-1000-10-1000) biopsy gun.
Model FNB and MBY single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue for example from pleura cavity and associated organs, abdominal cavity and associated organs like breast, liver, prostate and kidnev.
Model COX is for safe needle guidance and for taking several biopsy specimens. for example from liver, kidney, breast. thyroid, pancreas, spleen, lung and various soft tissue lesions, with only one single puncture.
Model ABG disposable automatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
Model SBG disposable semiautomatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
Model Möller Medical Blue RBG is a reusable, automatic biopsy gun that is intended exclusively for use with DNG-1020 / full-sCore® DNG-2020 disposable needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
When used for breast biopsy, the product is for diagnosis only. The extent of histological abnormality cannot be reliably determined from its mammographic appearance. Therefore, the extent of removal of the imaged evidence of an abnormality does not predict the extent of removal of a histological abnormality; e.g., malignancy. When the sampled abnormality is not histologically benign, it is essential that the tissue margins be examined for completeness of removal of
{3}------------------------------------------------
| | | using standard surgical procedures. | |
|--|--|-------------------------------------|--|
| | | | |
Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)
| | Over-The-Counter Use (21 CFR 801 Subpart C)
## CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{4}------------------------------------------------
Image /page/4/Picture/0 description: The image shows the logo for MöllerMedical. The logo consists of a stylized, light blue, four-petal flower-like design on the left. To the right of the design is the text "MöllerMedical" in a simple, sans-serif font, with "Möller" stacked above "Medical".
K162588 Traditional 510(k) Submission 510(k) Summary
Page: 1 (7)
# 510(k) Summary
| 1. Submitter | |
|-----------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Submitter: | Möller Medical GmbH<br>Wasserkuppenstrasse 29-31<br>36043 Fulda, Germany<br>Tel.: +49 (0) 661-94195-0<br>Fax: +49 (0) 661-94195-850 |
| | Establishment Registration Number: 3006611221 |
| Contact Person: | Grant Geckeler<br>Free lance consultant<br>1612 Jenks Drive<br>Corona, CA 92880<br>Phone: +1 858 603 1838<br>E-mail: grant.geckeler@gmail.com |
| Date Prepared: | September 01, 2016 |
| 2. Device | |
| Trade name: | Möller Medical Biopsy Needles and Systems<br>Consists of: Bone and Bone Marrow Aspiration Needles, Fine<br>Needles, Disposable Needles for Biopsy Guns, Coaxial<br>Needles, Manual Cut Biopsy Needles, Semi-automatic and<br>automatic Biopsy Guns |
| Common or Usual Name: | Biopsy Instruments |
| Classification Name: | Instrument Biopsy (21 CFR 876.1075) |
| Regulatory Class: | II |
| Product Code: | KNW |
{5}------------------------------------------------
Image /page/5/Picture/0 description: The image features the logo for "MöllerMedical". To the left of the text is a graphic of four light blue circles clustered together. The text "MöllerMedical" is in a simple, sans-serif font and is black.
Page: 2 (7)
#### 3. Predicate Device
The Möller Medical Biopsy Portfolio is coincident with other different biopsy products which are already FDA approved and distributed in the US market. Table 1 shows the identified appropriate predicate devices for the Möller Medical Biopsy Portfolio with the corresponding 510(k) number. The product codes and classes are also named.
#### Table 1: Predicate devices
| Möller Medical Product | Predicate Device with 510(k) No. | Code and<br>Class |
|-------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------|
| Möller Medical Blue Biopsy<br>Gun<br>(RBG-xxxx) | Pro-Mag Ultra 2.2 Automatic Biopsy<br>Instrument; Pro Mag Ultra Biopsy<br>Needles, Pro-Mag Ultra Automatic Biopsy<br>Instrument<br>510(k) No.: K980226 | KNW<br>Class II |
| Bone Marrow Biopsy<br>System<br>(BOW-1060) | Bone Marrow Aspiration Needles; Bone<br>Marrow Biopsy Trays; Bone Marrow<br>Harvest Needles; Osty-Core Bone Biopsy<br>Needles; Pediatric Bone Marrow Access<br>Needles; T-Lok Bone Marrow | KNW<br>Class II |
| Bone Marrow Aspiration<br>Biopsy<br>(BOW-1070) | Bone Marrow Aspiration Needles; Bone Marrow<br>Biopsy Trays; Bone Marrow Harvest<br>Needles; Osty-Core Bone Biopsy Needles<br>; Pediatric Bone Marrow Access Needles;<br>T-Lok Bone Marrow Needles | KNW<br>Class II |
| Bone Biopsy Needles<br>(BOY-1080) | 510(k) No.: K980196 | |
| Fine Needle Biopsy<br>(FNB-xxxx) | Fine Needle Aspiration (FNA) Biopsy<br>Needles Chiba; Franseen; Green;<br>MaxiCELL; Pro-Cut; Spinal; Trocar;<br>Turner; Westcott Soft Tissue Biopsy<br>Needles<br>510(k) No.: K980122 | KNW<br>Class II |
| Disposable Needles for<br>Biopsy Gun (DNG) | | |
| DNG-1010 | ACN, SACN, Biopsy Needle;<br>510(k) No.: K974446 | KNW<br>Class II |
| DNG-1020; DNG-1030 | Pro-Mag Ultra 2.2 Automatic Biopsy<br>Instrument; Pro-Mag Ultra Biopsy<br>Needles; Pro-Mag Ultra Automatic Biopsy<br>Instrument<br>510(k) No.: K980226 | KNW<br>Class II |
| DNG-1040 | Magnum Core Tissue Biopsy Needle<br>Model MN1820, RP Cutting Needle Model<br>RP-1820, MCN Core Tissue Biopsy<br>Needle Model MCN<br>510(k) No.: K111529 | KNW<br>Class II |
{6}------------------------------------------------
Image /page/6/Picture/0 description: The image shows the logo for MöllerMedical. The logo consists of a cluster of light blue circles on the left side. To the right of the circles is the text "MöllerMedical" in a sans-serif font.
K162588
Traditional 510(k) Submission
510(k) Summary
Page: 3 (7)
| Möller Medical Product | Predicate Device with 510(k) No. | Code and<br>Class |
|--------------------------------------------|-------------------------------------------------------------------------------------------------------------------------|-------------------|
| fullsCore® Biopsy Needle<br>(DNG-2020) | BioPince FullCore Biopsy Instrument<br>510(k) No.: K904987 | KNW<br>Class II |
| Semi-automatic Biopsy<br>Gun<br>(SBG-xxxx) | Speedybell<br>510(k) No.: K010735 | KNW<br>Class II |
| Automatic Biopsy Gun<br>(ABG-xxxx) | Manual-Bone-Marrow-Biopsy-Needles,<br>Semi-Automatic-Biopsy-Needles,<br>Automatic-Biopsy Needles<br>510(k) No.: K130616 | KNW<br>Class II |
| Coaxial Needles<br>(COX-xxxx) | Co-Axial Introducer Needle<br>510(k) No.: K980004 | KNW<br>Class II |
| Manual Cut Biopsy<br>(MBY-xxxx) | 18 Gauge Tru-Cut Biopsy Needle<br>510(k) No.: K960509 | KNW<br>Class II |
The presented Möller Medical products have the same indication and the same technology as the selected predicate devices.
#### 4. Device Description
#### Möller Medical Blue RBG
The Möller Medical Blue RBG is a re-usable biopsy gun to be used with corresponding needles to obtain core samples from soft tissue. It is a re-usable device, which has to be reprocessed. The biopsy needles used with this device are disposable products.
The Möller Medical Blue RBG is intended to be used with the DNG-1020 and the DNG-2020 needles.
The following steps are needed to prepare for the puncture. The first step is to open the cover of the Möller Medical Blue.
Generally spoken the insertion of biopsy needles into the re-usable biopsy gun is dependent from the biopsy needle. It is important that the plastic hubs of the compatible needles are positioned carefully onto the locking pins.
After needle insertion into the device the cover of the decocked re-usable biopsy gun shall be closed and the needle's protective sheath can be removed. By pulling the lever twice the device is ready for use and can be approached to the biopsy site - as a last step before triggering the safety lock has to switch from "locked" to "unlocked". Then introduce the needle under imaging control through the incision until the needle point is proximal to the area to be biopsied. When the position is confirmed the energized Möller Medical Blue RBG biopsy instrument hast to be triggered. Therefor the trigger button has to be depressed to cause both the stylet and cannula to automatically advance. Then the instrument has to be removed from the patient and the core tissue sample has to be exposed by pulling back the lever once from the side-notch. If additional biopsies are not being taken the used needle has
{7}------------------------------------------------
Image /page/7/Picture/0 description: The image shows the logo for MöllerMedical. The logo consists of a cluster of light blue circles on the left side, resembling a stylized molecule or a group of cells. To the right of the circles, the text "MöllerMedical" is written in a simple, sans-serif font. The text is black and appears to be the company's name.
Page: 4 (7)
to be removed from the decocked biopsy qun and discarded.
Bone Marrow Biopsy System (BOW-1060). Bone Marrow Aspiration Biopsy (BOW-1070) and Bone Biopsy Needles (BOY-1080):
The purpose of the Bone Marrow Biopsy System, Bone Marrow Aspiration Biopsy and Bone Biopsy Needles is the harvesting of bone and bone marrow specimens. Access to the bone or bone marrow is achieved manually under the support of the devices cutting edge. Harvesting of bone or bone marrow specimens is accomplished manually and if required by aspirating which a syringe which is adapted to the Luer-Lock connector located at the handle of the cannula. Specimens are collected within the outer cannula which finally will be withdrawn from the patient. The needle has to be inserted by a qualified physician under imaging guidance such as CT.
#### Fine Needle Biopsy (FNB-xxxx):
The Fine Needle Biopsy is used for the percutaneous withdrawal of mainly cytological evidence of soft tissue for example from pleura cavity and associated organs, abdominal cavity and associated organs. For aspiration a Luer-Lock adapter is attached on the top of the Needle to connect a syringe. The needle has to be inserted by a qualified physician under imaging guidance such as Ultrasound.
#### Disposable Needles for Biopsy Gun (DNG-1010, -1020, -1030, -1040):
The Disposable Needles for Biopsy Gun are used for obtaining core biopsies of various tissues like lung, kidney, liver, prostate, abdominal soft tissue masses and breast. The needles are used in combination with different automatic biopsy guns and can be used with a corresponding coaxial needle for multiple sampling.The needle has to be inserted by a qualified physician under imaging guidance such as Ultrasound or CT.
#### Full-sCore® Biopsy Needle (DNG-2020):
The full-sCore® Biopsy Needle is used for biopsies of soft tissue in combination with the Möller Medical Blue. These biopsy needles are composed of a double-lumen cannula tube with bevelled edge tip cut; a trokar stylet is located inside the larger lumen. The stylet also has a polished tip. The smaller lumen contains a lengthwise spade, which works as a cutting mechanisms for the tissue collected inside the needle. Full-sCore® can be used with a corresponding coaxial needle for multiple sampling. The needle has to be inserted by a qualified physician under imaging guidance such as Ultrasound or CT.
#### Semi-automatic Biopsy Gun (SBG-xxx):
The intended purpose of the disposable Semi-automatic Biopsy Gun is to obtain histological core samples from soft tissue such as liver, kidney, prostate, breast, lung and various soft tissue lesions. SBG-2010 is composed of an spring loaded biopsy needle fitted into a plastic handle permitting single handed specimen collection. The placement of the needle may be visualized by imaging quidance. SGB can be used with a corresponding coaxial needle for multiple sampling.The needle has to be inserted by a qualified physician under imaging quidance such as Ultrasound or CT.
{8}------------------------------------------------
Image /page/8/Picture/0 description: The image shows the logo for MöllerMedical. The logo consists of a light blue graphic to the left of the company name. The graphic is made up of four circles of varying sizes, arranged in a cluster. The company name, "MöllerMedical", is written in black, sans-serif font.
K162588 Traditional 510(k) Submission 510(k) Summary
Page: 5 (7)
#### Automatic Biopsy Gun (ABG-xxxx):
The intended purpose of the disposable Automatic Biopsy Gun of Möller Medical is to obtain core samples for valuable histological evidence from soft tissue such as liver, kidney. prostate, breast, lung and various soft tissue lesions. ABG can be used with a corresponding coaxial needle for multiple sampling. The needle has to be inserted by a qualified physician under imaging guidance such as Ultrasound or CT.
#### Coaxial Needles (COX-xxx):
If several biopsy specimens have to be taken from the same target area, the biopsies can be performed by means of several direct punctures or by using the coaxial technique. When performing direct punctures each and every time the biopsy needle or system has to be interseted into the patient. If a quiding needle is used together with the biopsy needle or system, this is known as coaxial approach. With this technique, only a single puncture is necessary. The quiding needle, the Coaxial Needle, is placed towards the suspicious area. Once the the coaxial needle is in place several biopsies can be performed by the biopsy needle or systems using the COX-xxxx as a guiding needle resp. as an introducer needle. It should be noted, that the guiding needle (COX) has to have a larger total diameter than the corresbonding biopsy needle or system and has to be shorter in length. The needle has to be inserted by a qualified physician under imaging guidance such as Ultrasound or CT.
#### Manual Cut Biopsy (MBY-xxxx):
The Manual Cut Biopsy needle is a manual biopsy needle for the evidence of histological tissue specimen. As with ABG, SBG and DNG the tru-cut technique is used in MBY. The needle has to be inserted by a qualified physician under imaging quidance such as Ultrasound or CT.
#### 5. Indications for Use
The Möller Medical Biopsy Needles and Systems are used to obtain core samples and aspiration from tissue by biopsy. The various wall thicknesses, diameters, tip geometries and cutting techniques of the different hollow needle types and biopsy systems affect the quality of the biopsy specimen.
Model BOW-1060 bone marrow biopsy systems are intended for the atraumatic taking of specimens from and inside bones. Application areas of the products are bone respectively bone marrow.
Model BOW-1070 bone marrow aspiration biopsy set is intended for aspiration in the area of the sternum or iliac crest. Application areas of the products are bone respectively bone marrow.
Model BOY-1080 bone biopsy needle set has been designed for atraumatic bone biopsy. Application areas of the products are bone respectively bone marrow.
Model DNG-10XX single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions and are combined with biopsy quns.
Model full-sCore® DNG-2020 disposable biopsy needles are intended only for biopsies on soft tissue and tissue from soft, internal organs such as liver, kidney, breast, lung and various
{9}------------------------------------------------
Image /page/9/Picture/1 description: The image contains the logo for MöllerMedical. The logo consists of a light blue abstract shape resembling a cluster of cells or molecules on the left. To the right of the shape is the text "MöllerMedical" in a simple, sans-serif font.
soft tissue lesions , and should be used with the Möller Medical Blue (RBG-1000-10-1000) biopsy gun.
Model FNB and MBY single-use biopsy needles are exclusively intended for hollow needle biopsies of soft tissue for example from pleura cavity and associated organs, abdominal cavity and associated organs like breast, liver, prostate and kidney,
Model COX is for safe needle guidance and for taking several biopsy specimens, for example from liver, kidney, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions, with only one single puncture.
Model ABG disposable automatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
Model SBG disposable semiautomatic biopsy guns are intended for biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
Model Möller Medical Blue RBG is a reusable, automatic biopsy gun that is intended exclusively for use with DNG-1020 / full-sCore® DNG-2020 disposable needles for core needle biopsies of soft tissue such as liver, kidney, prostate, breast, thyroid, pancreas, spleen, lung and various soft tissue lesions.
When used for breast biopsy, the product is for diagnosis only. The extent of histological abnormality cannot be reliably determined from its mammographic appearance. Therefore, the extent of removal of the imaged evidence of an abnormality does not predict the extent of removal of a histological abnormality; e.g., malignancy. When the sampled abnormality is not histologically benign, it is essential that the tissue margins be examined for completeness of removal of using standard surgical procedures.
#### 6. Comparison of Technological Characteristics with the Predicate Devices
The BiopC Portfolio is working equivalently to the predicate devices. The principles of biopsy are exactly the same.
With exception of the Möller Medical Blue RBG Biopsy gun the products are for single-use like the appropriate predicate devices.
The BiopC Portfolio and its predicate devices are sold sterile with exception of the Möller Medical Blue RBG which is suitable for reprocessing like the appropriate predicate device.
The indication for use of the BiopC Portfolio is comparable with the indication for use of the predicate devices.
#### 7. Performance Data
The BiopC Portfolio has the same indication for use and performance as the predicate devices. In addition, the BiopC Portfolio is made from the same materials with patient contact as the predicate devices. Because of this, no new safety or effectiveness are introduces over the predicate devices. Please refer to Table 2 for the list of bench tests - there you find a list of all bench tests that have been performed. Other products of the BiopC Portfolio can be subordinated to the bench tests of the single products.
The test series exhibits a very wide range of performance tests and all necessary and required tests for the BiopC Portfolio were appropriate performed and all tests passed according to the predetermined pass/fail criteria.
{10}------------------------------------------------
Image /page/10/Picture/0 description: The image shows the logo for MöllerMedical. The logo consists of a light blue abstract shape resembling a cluster of cells or a stylized flower. To the right of the abstract shape is the text "MöllerMedical" in a simple, sans-serif font. The text is black and appears to be the company's name.
Page: 7 (7)
#### Table 2: List of bench test
| Test | Tested<br>Products | Test method summary | |
|-------------------------|--------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---|
| Intensity Test | RBG | Test for preclearance of the Biopsy Gun | ✓ |
| Shelf Life | DNG | Test of tensile strength, impact strength and<br>functionality after 5 years | ✓ |
| Artificial Ageing | DNG | Comparison new- 2 years - 5 years | ✓ |
| Firing Test | DNG | Firing test with Biopsy Gun | ✓ |
| Validation/Verification | DNG | Firing test with smallest widening tolerance | ✓ |
| Firing test | DNG | Test of minimum pull-out force | ✓ |
| Functionality test | DNG-2020 | Function after 50 insertions per needle | ✓ |
| Performance test | All needles | Comparison of the general function, penetration<br>characteristics, tissue sample size and mechanical<br>durability of the different needles with the predicate<br>devices | ✓ |
#### 8. Conclusion
The BiopC Portfolio is equivalent to the predicate devices in that:
- The devices have the same intended use and indication for use.
- The devices have equivalent design, function and areas of application
- The devices demonstrate equivalent performance.
Predicate graph will load when search results are available.
Embedding visualization will load when search results are available.
PDF viewer will load when search results are available.
Loading panels...
Select an item from Submissions
Click any panel, subpart, regulation, product code, or device to see details here.
Section Matches
Results will appear here.
Product Code Matches
Results will appear here.
Special Control Matches
Results will appear here.
Loading collections...
Loading
My Alerts
You will receive email notifications based on the filters and frequency you set for each alert.
Sort by:
Create Alert
Search Filters
Agent Token
Create a read-only bearer token for Claude, ChatGPT, or other agents that can call HTTP APIs.
Copy this now. It will not be shown again.
Connected apps
Apps you authorized through browser sign-in. Disconnecting revokes their access immediately.
Learn the FDA Browser
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.