← Product Code [IZI](/productcode/IZI) · K130842 # ALLURA XPER FD OR TABLE SERIES; ALLURA XPER FD10 SERIES; ALLURA XPER FD20 SERIES; ALLURA XPER FD BIPLANE SERIES (K130842) _Philips Medical Systems Nederland B.V. · IZI · May 21, 2013 · Radiology · SESE_ **Canonical URL:** https://fda-staging.innolitics.com/device/K130842 ## Device Facts - **Applicant:** Philips Medical Systems Nederland B.V. - **Product Code:** [IZI](/productcode/IZI.md) - **Decision Date:** May 21, 2013 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 892.1600 - **Device Class:** Class 2 - **Review Panel:** Radiology - **Attributes:** 3rd-Party Reviewed ## Indications for Use The proposed Allura Xper FD X-ray imaging systems with the SSD spacer removed and the currently marketed and predicate Allura Xper FD X-ray imaging systems with the SSD spacer mounted are indicated for use on human patients to perform: - Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal angiography, as well as PTAs, stent placements, embolisations and thrombolysis. - Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA, stent placing, atherectomies), pacemaker implantations, and electrophysiology (EP). - Non-vascular interventions such as drainages, biopsies and vertebroplasties procedures. Combined with a qualified, compatible Operating Room (OR) table, the Allura Xper FD OR Table X-ray imaging systems can be used for imaging in the hybrid OR within the applications domains neuro, vascular, non-vascular and cardiac. The OR table can also be used stand-alone for surgical use in the OR. ## Device Story Allura Xper FD series are X-ray imaging systems for diagnostic and interventional procedures. This modification involves removing the source-skin distance (SSD) spacer from the X-ray tube housing. Removal facilitates mounting of external mapping system frames (e.g., BioSense Webster CARTO) beneath the patient table for electrophysiology procedures, preventing interference with C-arc rotation. The system maintains a minimum SSD of 30 cm, complying with IEC 60601-2-43, IEC 60601-2-54, and 21 CFR 1020.32(g). Operated by clinicians in hybrid ORs or interventional suites, the system provides real-time X-ray imaging to guide minimally invasive interventions. Output is visualized by the physician to assist in navigation and procedural decision-making, potentially improving patient outcomes by enabling complex electrophysiology and vascular interventions. ## Clinical Evidence Bench testing only. The manufacturer states that removal of the SSD spacer has no effect on the performance of the X-ray tube, collimator, flat solid-state detector, hardware, or software. No clinical data was required or provided. ## Technological Characteristics Angiographic X-ray system. Components include X-ray tube, collimator, and flat solid-state X-ray detector. Minimum source-skin distance (SSD) is 30 cm. Complies with IEC 60601-2-43 and IEC 60601-2-54. System is designed for integration with OR tables in hybrid surgical environments. ## Regulatory Identification An angiographic x-ray system is a device intended for radiologic visualization of the heart, blood vessels, or lymphatic system during or after injection of a contrast medium. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories. ## Predicate Devices - Allura Xper FD OR Table series ([K102005](/device/K102005.md)) - Allura Xper FD10 series ([K041949](/device/K041949.md)) - Allura Xper FD20 series ([K033737](/device/K033737.md)) - Integris Series Release 2 ([K984545](/device/K984545.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ ## 尺 130 84 2 1 - . # MAY 2 1 2013 ### 510(k) Summary of Safety and Effectiveness . | Device Name: | The proposed Allura Xper FD X-ray imaging systems with the SSD spacer
removed include the following:
• Allura Xper FD OR Table series;
• Allura Xper FD10 series;
• Allura Xper FD20 series;
• Allura Xper FD Biplane series. | |---------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Classification: | Classification Name: 21 CFR, Part 892.1600 - Angiographic x-ray system
Classification: Class II
Classification Panel: Radiology
Product Code: IZI | | Date Prepared: | January 18, 2013 | | Sponsor: | Philips Medical Systems Nederland B. V.
Veenpluis 4-6
5684PC Best
The Netherlands | | Contact: | Dr. Jos van Vroonhoven
Standardization manager | | Predicate Devices: | The predicate devices of the proposed Allura Xper FD X-ray imaging systems
with the SSD spacer removed include the following Allura Xper FD X-ray
imaging systems with the SSD spacer mounted (also manufactured and marketed
by Philips Medical Systems Nederland B.V.):
• Allura Xper FD OR Table series (K102005 - cleared by FDA on August
9, 2010);
• Allura Xper FD10 series (K041949 - cleared by FDA on July 30, 2004);
• Allura Xper FD20 series (K033737 - cleared by FDA on December 9,
2003);
• Integris Series Release 2 (K984545 - cleared by FDA on February 25,
1999). Note: the Integris Series Release 2 systems are currently marketed
as Allura Xper FD Biplane series. | | Device Description: | The proposed Allura Xper FD X-ray imaging systems with the SSD spacer
removed are identical to the currently marketed and predicate Allura Xper FD
X-ray imaging systems with the source-skin distance spacer (SSD spacer)
mounted onto the X-ray tube housing, except that the SSD spacer is removed.
Removal of the SSD spacer allows the execution of electrophysiology (EP)
surgical procedures that require mounting of a special frame of currently
marketed mapping systems (such as BioSense Webster's CARTO frame or
Location Pad, etc.) underneath the patient table. With the BioSense Webster's
CARTO frame mounted underneath the patient table, the SSD spacer mounted
onto the X-ray tube housing of the currently marketed and predicate Allura Xper | {1}------------------------------------------------ FD X-ray imaging systems interferes with the C-arc rotations during EP procedures, thus necessitating the removal of the SSD spacer. By construction, the source-skin distance cannot become smaller than 30 cm when the SSD spacer is removed. This minimum SSD complies with the international product safety standards IEC 60601-2-43 and IEC 60601-2-54 and with the minimum distance of 20 cm as required per 21 CFR, Part 1020.32(g) for certain specific surgical procedures. Intended Use: The proposed Allura Xper FD X-ray imaging systems with the SSD spacer removed and the currently marketed and predicate Allura Xper FD X-ray imaging systems with the SSD spacer mounted are indicated for use on human patients to perform: - Vascular, cardiovascular and neurovascular imaging applications, including . diagnostic, interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal angiography, as well as PTAs, stent placements, embolisations and thrombolysis. - Cardiac imaging applications including diagnostics, interventional and . minimally invasive procedures (such as PTCA, stent placing, atherectomies), pacemaker implantations, and electrophysiology (EP). - . Non-vascular interventions such as drainages, biopsies and vertebroplasties procedures. Combined with a qualified, compatible Operating Room (OR) table, the Allura Xper FD OR Table X-ray imaging systems can be used for imaging in the hybrid OR within the applications domains neuro, vascular, non-vascular and cardiac. The OR table can also be used stand-alone for surgical use in the OR. . Non-clinical Test Data: The performance of the proposed Allura Xper FD X-ray systems with the SSD spacer removed is equivalent to the performance of the currently marketed and predicate Allura Xper FD X-ray imaging systems, since the removal of the SSD spacer has no effect on the performance of the X-ray tube, the collimator, the flat solid-state X-ray detector, the hardware and the software. #### Substantial Equivalence The proposed Allura Xper FD X-ray imaging systems with the SSD spacer to Predicate Devices: removed are substantially equivalent to the currently marketed and predicate Allura Xper FD X-ray imaging systems with the SSD spacer mounted, in terms of design, indications for use, principle of operations, performance, hardware and software. {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES USA" arranged around the perimeter. Inside the circle is a stylized symbol that resembles a caduceus, a traditional symbol of medicine, but with three lines instead of one. #### DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 May 21, 2013 Philips Medical Systems Nederland B.V. % Dr. Jos Van Vroonhoven Veenpluis 4-6 5684 PC Best NETHERLANDS Re: K130842 Trade/Device Name: Allura Xper FD series with the SSD spacer removed Regulation Number: 21 CFR 892.1600 Regulation Name: Angiographic x-ray system Regulatory Class: Class II Product Code: IZI Dated: January 29, 2013 Received: April 22, 2013 Dear Dr. Vroonhoven: 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 (reporting of medical {3}------------------------------------------------ Page 2 - Dr. Vroonhoven device-related 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. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree 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" (21CFR 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 Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Sincerely vours. Michael D. O'Hara for Janine M. Morris Director, Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## Indications for Use 510(k) Number (if known): K130842 Device Name: Allura Xper FD series with the SSD spacer removed Indications for Use: The Allura Xper FD X-ray imaging systems are indicated for use on human patients to perform: - Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, . interventional and minimally invasive procedures. This includes, e.g., peripheral, cerebral, thoracic and abdominal angiography, as well as PTAs. stent placements, embolisations and thrombolysis. - . Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as PTCA, stent placing, atherectomies), pacemaker implantations, and electrophysiology (EP). - Non-vascular interventions such as drainages, biopsies and vertebroplasties procedures. . Combined with a qualified, compatible Operating Room (OR) table, the Allura Xper FD OR Table X-ray imaging systems can be used for imaging in the hybrid OR within the application domains neuro, vascular, non-vascular and cardiac. The OR table can also be used stand-alone for surgical use in the OR. Prescription Use YES . (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use NO (21 CFR 807 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of In Vitro Diagnostics and Radiological Health (OIR) Michael D. O'Hara (Division Sign Off) Division of Radiological Health Office of In Vitro Diagnostics and Radiological Health K130842 510(k) Page 1 of 1 --- **Source:** [https://fda-staging.innolitics.com/device/K130842](https://fda-staging.innolitics.com/device/K130842) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com