Smith and Nephew Suture Anchors - 5.0mm Absorbable Polymer Anchor, Smith and Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317, 7209318, Smith and Nephew Suture Anchors - Bioraptor 2.3 PK Suture Anchor, Smith and Nephew Suture Anchors - Osteoraptor Suture Anchor, Smith and Nephew Suture Anchors - Twinfix Ultra HA Suture Anchor, Smith and Nephew Suture Anchors - OSTEORAPTOR Curved Suture Anchors, Smith and Nephew Suture Anchors - Ultra Fast-Fix Meniscal Repair System, Ultra Fa
K151105 · Smith & Nephew, Inc. · MAI · Jul 28, 2015 · Orthopedic
Device Facts
Record ID
K151105
Device Name
Smith and Nephew Suture Anchors - 5.0mm Absorbable Polymer Anchor, Smith and Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317, 7209318, Smith and Nephew Suture Anchors - Bioraptor 2.3 PK Suture Anchor, Smith and Nephew Suture Anchors - Osteoraptor Suture Anchor, Smith and Nephew Suture Anchors - Twinfix Ultra HA Suture Anchor, Smith and Nephew Suture Anchors - OSTEORAPTOR Curved Suture Anchors, Smith and Nephew Suture Anchors - Ultra Fast-Fix Meniscal Repair System, Ultra Fa
Applicant
Smith & Nephew, Inc.
Product Code
MAI · Orthopedic
Decision Date
Jul 28, 2015
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 888.3030
Device Class
Class 2
Attributes
Therapeutic
Indications for Use
The Smith & Nephew 5.0 Absorbable Polymer Anchor is intended for use only for the reattachment of soft tissue to bone for the following indications: Shoulder: 1. Bankart lesion repairs 2. SLAP lesion repairs 3. Acromioclavicular separation repairs 4. Rotator cuff tear repairs 5. Capsular shift or capsulolabral reconstructions 6. Biceps tenodesis 7. Deltoid repairs Foot and Ankle: 1. Hallux valgus repairs 2. Medial or lateral instability repairs/reconstructions 3. Achilles tendon repairs/reconstructions 4. Midfoot reconstructions 5. Metatarsal ligament/tendon repairs/reconstructions Elbow, Wrist, and Hand: 1. Scapholunate ligament reconstructions 2. Ulnar or radial collateral ligament reconstructions 3. Lateral epicondylitis repair 4. Biceps tendon reattachment Knee: 1. Extra-capsular repairs: a. Medial collateral ligament b. Lateral collateral ligament c. Posterior oblique ligament 2. Iliotibial band tenodesis 3. Patellar realignment and tendon repairs, including vastus medialis obliquous advancement
Device Story
Suture anchors for reattachment of soft tissue to bone; used in orthopedic procedures (shoulder, knee, hip, foot/ankle, elbow/wrist/hand). Devices consist of absorbable polymer anchors pre-assembled on inserters; some configurations include non-absorbable sutures, needles, guides, or dilators. Operated by surgeons in OR settings (percutaneous or endoscopic). Anchors provide mechanical fixation of soft tissue to bone; facilitate meniscal repair and allograft transplant. Benefit: secure tissue fixation during healing.
Clinical Evidence
Bench testing only. Performance data includes ship testing and post-shipment mechanical functional testing for insertion and pullout (fixation) force, demonstrating equivalence to predicate devices.
Technological Characteristics
Composite absorbable materials; pre-assembled on inserters; sterile, single-use. Includes configurations with non-absorbable sutures, stainless steel needles, guides, and threaded dilators. Mechanical fixation principle.
Indications for Use
Indicated for reattachment of soft tissue to bone in shoulder, elbow, wrist, hand, hip, knee, foot, and ankle procedures, including ligament/tendon repairs, reconstructions, and meniscal repair/allograft transplant.
Regulatory Classification
Identification
Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.
Predicate Devices
SMITH AND NEPHEW 5.00MM ABSORBABLE POLYMER ANCHOR (K011299)
TAG ROD BIORAPTOR SUTURE ANCHOR 7209317, 7209318 (K031685)
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Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is a circular seal with the words "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" around the perimeter. Inside the circle is an abstract image of a human face in profile, with three overlapping faces suggesting a sense of community and connection. The logo is black and white.
July 28, 2015
Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002
Smith & Nephew, Incorporated Ms. Katherine Marcaccio Regulatory Affairs Specialist II 150 Minuteman Road Andover, Massachusetts 01810
Re: K151105
Trade/Device Name: Smith and Nephew Suture Anchors - 5.0mm Absorbable Polymer Anchor; Smith and Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317; 7209318, Smith and Nephew Suture Anchors -Bioraptor 2.3 PK Suture Anchor; Smith and Nephew Suture Anchors - Osteoraptor Suture Anchor; Smith and Nephew Suture Anchors -Twinfix Ultra HA Suture Anchor; Smith and Nephew Suture Anchors - OSTEORAPTOR Curved Suture Anchors; Smith and Nephew Suture Anchors - Ultra Fast-Fix Meniscal Repair System; Ultra Fast-Fix AB Meniscal Repair System; Fast-Fix 360 Meniscal Repair System; Smith and Nephew Suture Anchors - Healicoil Absorbable Suture Anchor Regulation Number: 21 CFR 888.3030 Regulation Name: Single/multiple component metallic bone fixation appliances and accessories Regulatory Class: Class II Product Code: MAI, HWC, JDR, MBI, GAT
Dear Ms. Marcaccio:
Dated: April 22, 2015 Received: April 24, 2015
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.
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#### Page 2 - Ms. Katherine Marcaccio
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 device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (OS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
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 yours,
# Mark N. Melkerson -S
Mark N. Melkerson Director Division of Orthopedic Devices Office of Device Evaluation Center for Devices and Radiological Health
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510(k) Number (if known): ________________
Smith & Nephew Suture Anchors – 5.0mm Absorbable Polymer Anchor Device Name:
Indications for Use:
The Smith & Nephew 5.0 Absorbable Polymer Anchor is intended for use only for the reattachment of soft tissue to bone for the following indications:
| Shoulder: | Elbow, Wrist, and Hand: |
|----------------------------------------------------------|---------------------------------------------------------------------------------------------|
| 1. Bankart lesion repairs | 1. Scapholunate ligament reconstructions |
| 2. SLAP lesion repairs | 2. Ulnar or radial collateral ligament reconstructions |
| 3. Acromioclavicular separation repairs | 3. Lateral epicondylitis repair |
| 4. Rotator cuff tear repairs | 4. Biceps tendon reattachment |
| 5. Capsular shift or capsulolabral reconstructions | |
| 6. Biceps tenodesis | |
| 7. Deltoid repairs | |
| Foot and Ankle: | Knee: |
| 1. Hallux valgus repairs | 1. Extra-capsular repairs: |
| 2. Medial or lateral instability repairs/reconstructions | a. Medial collateral ligament |
| 3. Achilles tendon repairs/reconstructions | b. Lateral collateral ligament |
| 4. Midfoot reconstructions | c. Posterior oblique ligament |
| 5. Metatarsal ligament/tendon repairs/reconstructions | 2. Iliotibial band tenodesis |
| | 3. Patellar realignment and tendon repairs, including vastus medialis obliquous advancement |
Prescription Use ___X____ AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use _ (Part 21 CFR 801 subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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510(k) Number (if known): ___________
Device Name: Smith & Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317, 7209318
Indications for Use:
- 1. Bankart Lesion Repair
- 2. Rotator Cuff Repair
- 3. Capsular Stabilization
- 4. Anterior Shoulder Instability Repair
- 5. Repair of ligaments and tendons of the elbow, foot, and ankle including the treatment of:
- Bunionectomy
- Lateral ankle instability ।
- Biceps tendon reattachment -
Prescription Use X AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use _ (Part 21 CFR 801 subpart C)
#### (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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Smith & Nephew Suture Anchors - Bioraptor 2.3 PK Suture Anchor Device Name:
Indications for Use:
These suture anchors are intended for the fixation of soft tissue to bone in the Hip, Shoulder, Foot, Ankle, Elbow, Wrist, Hand and Knee as follows:
#### Hip:
Hip capsule repair
। Acetabular labrum reattachment
#### Shoulder:
Capsular stabilization
- Bankart repair -
- -Anterior shoulder instability
- SLAP lesion repairs -
- Capsular shift or capsulolabral reconstructions
Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
# Elbow, Wrist, and Hand:
Biceps tendon reattachment Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair
#### Knee:
Extra-capsular repairs:
- Medial collateral ligament -
- -Lateral collateral ligament
- -Posterior oblique ligament
Patellar realignment and tendon repairs
- Vastus medialis obliquous advancement Iliotibial band tenodesis
#### Foot and Ankle:
Hallux valgus repairs Medial or lateral instability repairs/ reconstructions Achilles tendon repairs/reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions Bunionectomy
Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use (Part 21 CFR 801 subpart C)
#### (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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Smith & Nephew Suture Anchors – Osteoraptor Suture Anchor Device Name:
Indications for Use:
The Smith & Nephew OSTEORAPTOR Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
#### Elbow, Wrist, and Hand
Biceps tendon reattachment Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair
### Foot and Ankle
Hallux valgus repairs Medial or lateral instability repairs/ reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions Bunionectomy
#### Hip
Hip capsule repair
- Acetabular labrum reattachment
### Knee
Extra-capsular repairs:
- Medial collateral ligament -
- -Lateral collateral ligament
- Posterior oblique ligament -
Patellar realignment and tendon repairs
- Vastus medialis obliquous advancement Iliotibial band tenodesis
### Shoulder
Capsular stabilization
- -Bankart repair
- Anterior shoulder instability -
- SLAP lesion repairs -
- -Capsular shift or capsulolabral reconstructions
Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use _ (Part 21 CFR 801 subpart C)
#### (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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510(k) Number (if known): ____________________________________________________________________________________________________________________________________________________
Smith & Nephew Suture Anchors – Twinfix Ultra HA Suture Anchor Device Name:
Indications for Use:
The Smith & Nephew TWINFIX Ultra HA Suture Anchor is intended for use for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
- Bankart repairs SLAP lesion repairs Capsular shift or capsulolabral reconstructions Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
#### Foot and Ankle:
Hallux valgus repairs Medial or lateral instability repairs/reconstructions Achilles tendon repairs/reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions
### Knee:
Extra-capsular repairs:
- । Medial collateral ligament
- Lateral collateral ligament -
- Posterior oblique ligament -
Patellar realignment and tendon repairs:
Vastus medialis obliquous advancement । Iliotibial band tenodesis
#### Elbow:
Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair Biceps tendon reattachment
AND/OR Prescription Use _____________________________________________________________________________________________________________________________________________________________ (Part 21 CFR 801 subpart D)
Over-the-Counter Use (Part 21 CFR 801 subpart C)
#### (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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510(k) Number (if known): ________________
Device Name: Smith & Nephew Suture Anchors – OSTEORAPTOR Curved Suture Anchors
Indications for Use:
The Smith & Nephew OSTEORAPTOR Curved Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
Capsular stabilization
- -Bankart repair
- Anterior shoulder instability -
- -SLAP lesion repairs
- Capsular shift or capsulolabral . reconstructions
Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs
Biceps tenodesis
Prescription Use _____________________________________________________________________________________________________________________________________________________________ AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use _ (Part 21 CFR 801 subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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Device Name: Smith & Nephew Suture Anchors – Ultra Fast-Fix Meniscal Repair System, Ultra Fast-Fix AB Meniscal Repair System, Fast-Fix 360 Meniscal Repair System
Indications for Use:
The ULTRA FAST-FIX Meniscal Repair System is intended for use as suture retention devices to facilitate percutaneous or endoscopic soft tissue procedures. The ULTRA FAST-FIX System is indicated for use in meniscal repairs and allograft transplant procedures. The ULTRA FAST-FIX System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
The ULTRA FAST-FIX AB Meniscal Repair System is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The ULTRA FAST-FIX AB System is indicated for use in meniscal repairs and allograft transplant procedures. The ULTRA FAST-FIX AB System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
The FAST-FIX 360 Meniscal Repair System is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The FAST-FIX 360 System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
Prescription Use X AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use (Part 21 CFR 801 subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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Smith & Nephew Suture Anchors – Healicoil Absorbable Suture Anchor Device Name:
Indications for Use:
Bankart lesion repairs
Rotator cuff tear repairs
Slap lesion repairs
The Smith & Nephew HEALICOIL Absorbable Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
Knee:
Extra-capsular repairs:
- Medial collateral ligament ।
- -Lateral collateral ligament
- Posterior oblique ligament -
Patellar realignment and tendon repairs:
Vastus medialis obliquous advancement -Iliotibial band tenodesis
### Foot and Ankle:
Biceps tenodesis
Deltoid repairs
Hallux valgus repairs Medial or lateral instability repairs/reconstructions Achilles tendon repairs/reconstruction Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions
Capsular shift or capsulolabral reconstructions
Acromioclavicular separation repairs
### Elbow:
Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair Biceps tendon reattachment
Prescription Use AND/OR (Part 21 CFR 801 subpart D)
Over-the-Counter Use (Part 21 CFR 801 subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE – CONTINUE ON ANOTHER PAGE IF NEEDED)
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# 510(k) Summary
# Date Prepared: May 15, 2015
| Submitter Information | Contact Information |
|-----------------------|----------------------------------|
| Smith & Nephew, Inc. | Katherine Marcaccio |
| 150 Minuteman Road | Regulatory Affairs Specialist II |
| Andover, MA 01810 | Phone: (508) 261-3602 |
| | Fax: (978) 749-1443 |
| Device Name (Unmodified) | |
|---------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Trade or proprietary name | Smith & Nephew Absorbable Suture Anchors |
| Common or usual name | HWC - Screw, Fixation, Bone<br>JDR - Staple, Fixation, Bone<br>MAI - Fastener, Fixation, Biodegradable, Soft Tissue<br>MBI - Fastener, Fixation, Nondegradable, Soft Tissue<br>GAT - Suture, Nonabsorbable, Synthetic, Polyethylene |
| Classification name | 21 CFR §888.3030 – Single/multiple component metallic bone<br>fixation appliances and accessories<br>21 CFR §888.3040 – Smooth or threaded metallic bone<br>fixation fastener<br>21 CFR §878.5000 - Nonabsorbable poly(ethylene<br>terephthalate) surgical suture |
# Legally Marketed Predicate Device
The Smith & Nephew Absorbable Suture Anchors are substantially equivalent in intended use and Fundamental Scientific Technology to the following legally marketed devices in commercial distribution:
| 510(k)<br>Number | Device Name | Clearance<br>Date |
|------------------|----------------------------------------------------------------------------------------------------|-------------------|
| K011299 | SMITH AND NEPHEW 5.00MM ABSORBABLE POLYMER<br>ANCHOR | 06/27/2001 |
| K031685 | TAG ROD BIORAPTOR SUTURE ANCHOR 7209317, 7209318 | 07/01/2003 |
| K071586 | Bioraptor 2.3 PK Suture Anchor | 08/17/2007 |
| K082215 | Osteoraptor Suture Anchor | 11/03/2008 |
| K093844 | SMITH & NEPHEW TWINFIX ULTRA HA SUTURE ANCHOR | 04/01/2010 |
| K103309 | OSTEORAPTOR Curved Suture Anchors | 02/03/2011 |
| K121861 | SMITH & NEPHEW ULTRA FAST-FIX MENISCAL REPAIR<br>SYSTEM, SMITH & NEPHEW ULTRA FAST-FIX AB MENISCAL | 10/18/2012 |
{11}------------------------------------------------
| | REPAIR SYSTEM, SMITH & NEPHEW FAST-FIX 360 MENISCAL<br>REPAIR SYSTEM | |
|---------|----------------------------------------------------------------------|------------|
| K123393 | HEALICOIL SUTURE ANCHOR WITH REGENESORB | 04/11/2013 |
#### Device Description
Smith & Nephew Absorbable Suture Anchors are provided in various composite absorbable materials. All of the Smith & Nephew Absorbable Suture Anchors are provided sterile, for single use only. All Smith & Nephew Absorbable Suture Anchors are pre-assembled onto an inserter, sized appropriately to accommodate the indicated procedures. Smith & Nephew Absorbable Suture Anchors come in various configurations, including: with attached non-absorbable suture(s), and with attached stainless steel needle(s). In certain configurations, the Absorbable Suture Anchors are packaged with a guide and threaded dilator. All configurations of the Absorbable Suture Anchors are identical to the identified predicate devices.
#### Intended Use
#### Smith & Nephew Suture Anchors – 5.0mm Absorbable Polymer Anchor
The Smith & Nephew 5.0 Absorbable Polymer Anchor is intended for use only for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
- 1. Bankart lesion repairs
- SLAP lesion repairs 2.
- Acromioclavicular separation repairs ဒေ
- Rotator cuff tear repairs 4.
- 5. Capsular shift or capsulolabral reconstructions
- 6. Biceps tenodesis
- 7. Deltoid repairs
#### Foot and Ankle:
- 1. Hallux valgus repairs
- Medial or lateral instability 2. repairs/reconstructions
- 3. Achilles tendon repairs/reconstructions
- 4. Midfoot reconstructions
- 5. Metatarsal ligament/tendon repairs/reconstructions
#### Elbow, Wrist, and Hand:
- 1. Scapholunate ligament reconstructions
- 2. Ulnar or radial collateral ligament reconstructions
- ဒေ Lateral epicondylitis repair
- 4. Biceps tendon reattachment
- Knee:
- 1. Extra-capsular repairs:
- a. Medial collateral ligament
- b. Lateral collateral ligament
- Posterior oblique ligament ﻥ
- 2. Illiotibial band tenodesis
- 3. Patellar realignment and tendon repairs, including vastus medialis obliquous advancement
{12}------------------------------------------------
#### Smith & Nephew Suture Anchors - TAG Bioraptor Suture Anchor 7209317, 7209318
- Bankart Lesion Repair 1.
- 2. Rotator Cuff Repair
- Capsular Stabilization 3.
- Anterior Shoulder Instability Repair 4.
- 5. Repair of ligaments and tendons of the elbow, foot, and ankle including the treatment of:
- Bunionectomy -
- Lateral ankle instability -
- Biceps tendon reattachment -
# Smith & Nephew Suture Anchors - Bioraptor 2.3 PK Suture Anchor
These suture anchors are intended for the fixation of soft tissue to bone in the Hip, Shoulder, Foot, Ankle, Elbow, Wrist, Hand and Knee as follows:
# Hip:
Hip capsule repair
- -Acetabular labrum reattachment
# Shoulder:
Capsular stabilization
- -Bankart repair
- Anterior shoulder instability -
- -SLAP lesion repairs
- Capsular shift or capsulolabral reconstructions
- Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
# Foot and Ankle:
- Hallux valgus repairs Medial or lateral instability repairs/ reconstructions Achilles tendon repairs/reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions Bunionectomy
# Elbow, Wrist, and Hand:
Biceps tendon reattachment Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair
# Knee:
Extra-capsular repairs:
- Medial collateral ligament -
- Lateral collateral ligament -
- -Posterior oblique ligament
- Patellar realignment and tendon repairs
- -Vastus medialis obliquous
- advancement
- Iliotibial band tenodesis
{13}------------------------------------------------
#### Smith & Nephew Suture Anchors - Osteoraptor Suture Anchor
The Smith & Nephew OSTEORAPTOR Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
### Elbow, Wrist, and Hand
Biceps tendon reattachment Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair
# Foot and Ankle
Hallux valgus repairs Medial or lateral instability repairs/ reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions Bunionectomy
# Hip
Hip capsule repair
Acetabular labrum reattachment -
## Knee
Extra-capsular repairs:
- Medial collateral ligament
- -Lateral collateral ligament
- -Posterior oblique ligament
Patellar realignment and tendon repairs
- Vastus medialis obliquous
- advancement
Iliotibial band tenodesis
# Shoulder
Capsular stabilization
- -Bankart repair
- Anterior shoulder instability -
- SLAP lesion repairs -
- -Capsular shift or capsulolabral reconstructions
Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
{14}------------------------------------------------
#### Smith & Nephew Suture Anchors - Twinfix Ultra HA Suture Anchor
The Smith & Nephew TWINFIX Ultra HA Suture Anchor is intended for use for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
Bankart repairs SLAP lesion repairs Capsular shift or capsulolabral reconstructions Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
# Foot and Ankle:
Hallux valgus repairs Medial or lateral instability repairs/reconstructions Achilles tendon repairs/reconstructions Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions
#### Knee:
Extra-capsular repairs:
- Medial collateral ligament -
- Lateral collateral ligament -
- Posterior oblique ligament -
Patellar realignment and tendon repairs:
-Vastus medialis obliquous advancement Iliotibial band tenodesis
### Elbow:
Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair Biceps tendon reattachment
Smith & Nephew Suture Anchors – OSTEORAPTOR Curved Suture Anchors The Smith & Nephew OSTEORAPTOR Curved Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
#### Shoulder:
Capsular stabilization
- -Bankart repair
- Anterior shoulder instability -
- SLAP lesion repairs -
- Capsular shift or capsulolabral reconstructions
Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
{15}------------------------------------------------
#### Smith & Nephew Suture Anchors – Ultra Fast-Fix Meniscal Repair System, Ultra Fast-Fix AB Meniscal Repair System, Fast-Fix 360 Meniscal Repair System
The ULTRA FAST-FIX Meniscal Repair System is intended for use as suture retention devices to facilitate percutaneous or endoscopic soft tissue procedures. The ULTRA FAST-FIX System is indicated for use in meniscal repairs and allograft transplant procedures. The ULTRA FAST-FIX System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
The ULTRA FAST-FIX AB Meniscal Repair System is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The ULTRA FAST-FIX AB System is indicated for use in meniscal repairs and allograft transplant procedures. The ULTRA FAST-FIX AB System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
The FAST-FIX 360 Meniscal Repair System is intended for use as a suture retention device to facilitate percutaneous or endoscopic soft tissue procedures. The FAST-FIX 360 System is intended to be used for anchoring the allograft to the meniscal rim during allograft transplant procedures.
Smith & Nephew Suture Anchors - Healicoil Absorbable Suture Anchor The Smith & Nephew HEALICOIL Absorbable Suture Anchor is intended for the reattachment of soft tissue to bone for the following indications:
# Shoulder:
Bankart lesion repairs Slap lesion repairs Capsular shift or capsulolabral reconstructions Acromioclavicular separation repairs Deltoid repairs Rotator cuff tear repairs Biceps tenodesis
# Foot and Ankle:
Hallux valgus repairs Medial or lateral instability repairs/reconstructions Achilles tendon repairs/reconstruction Midfoot reconstructions Metatarsal ligament/tendon repairs/reconstructions
# Knee:
Extra-capsular repairs:
- Medial collateral ligament -
- Lateral collateral ligament -
- Posterior oblique ligament ।
Patellar realignment and tendon repairs:
Vastus medialis obliquous advancement -Iliotibial band tenodesis
# Elbow:
Ulnar or radial collateral ligament reconstructions Lateral epicondylitis repair Biceps tendon reattachment
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#### Technological Characteristics
Smith & Nephew Absorbable Suture Anchors are substantially equivalent in intended use and fundamental scientific technology to the legally marketed predicate devices in this submission and raises no new issues of safety and efficacy.
#### Summary of Performance Data
Ship Testing and Post-Shipment mechanical functionaltesting for insertion and pullout (fixation) force demonstrates that the Absorbable Suture Anchors are substantially equivalent to the currently marketed predicate devices.
#### Substantial Equivalence Information
The substantial equivalence of the Absorbable Suture Anchors is based on identical indications for use, design features, operational principles, material composition, and performance to the predicate devices listed above. Based on the identical features to the predicates, the Absorbable Suture Anchors are substantially equivalent to the predicates.
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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.