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FDA 510(k)

BePOD Cannulated Arthrodesis Screws

K-Number: K170040 · 2017-04-04

ApplicantFournitures Hospitalieres Industrie
Decision Date2017-04-04
Product CodeHWC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BePOD Cannulated Arthrodesis Screws is the device name listed in this FDA 510(k) record. The listed applicant is Fournitures Hospitalieres Industrie. It received FDA 510(k) clearance on 2017-04-04 under 510(k) number K170040. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BePOD Cannulated Arthrodesis Screws?

BePOD Cannulated Arthrodesis Screws is a medical device that received FDA 510(k) clearance on 2017-04-04. The listed applicant is Fournitures Hospitalieres Industrie. The 510(k) number is K170040.

When did BePOD Cannulated Arthrodesis Screws receive FDA 510(k) clearance?

BePOD Cannulated Arthrodesis Screws received FDA 510(k) clearance on 2017-04-04, under 510(k) number K170040.

Who is the listed applicant for BePOD Cannulated Arthrodesis Screws?

The FDA 510(k) record lists Fournitures Hospitalieres Industrie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BePOD Cannulated Arthrodesis Screws?

The FDA product code for BePOD Cannulated Arthrodesis Screws is HWC. This falls under the Cardiovascular category.

Other records listing Fournitures Hospitalieres Industrie as applicant

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Related Devices (Code: HWC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262344Large Compression ScrewsTriMed, Inc.K253858GFS - Sterile Screws and Top HatT.A.G. Medical Products Corporation, Ltd.K262075Lapidus Screw KitRelja Innovations, LLCK260809Arthrex Sterile VAL and VAL KreuLock™ Compression Screw SystemArthrex, Inc.K253108VEOFIX Snap Off ScrewSteps OrthoK261154CoLink® & CoLag® Non-Sterile ScrewsIn2Bones USA, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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