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FDA 510(k)

Arthrex SynergyID Endoscopic Imaging System

K-Number: K202582 · 2021-07-22

ApplicantArthrex, Inc.
Decision Date2021-07-22
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Arthrex SynergyID Endoscopic Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2021-07-22 under 510(k) number K202582. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Arthrex SynergyID Endoscopic Imaging System?

Arthrex SynergyID Endoscopic Imaging System is a medical device that received FDA 510(k) clearance on 2021-07-22. The listed applicant is Arthrex, Inc.. The 510(k) number is K202582.

When did Arthrex SynergyID Endoscopic Imaging System receive FDA 510(k) clearance?

Arthrex SynergyID Endoscopic Imaging System received FDA 510(k) clearance on 2021-07-22, under 510(k) number K202582.

Who is the listed applicant for Arthrex SynergyID Endoscopic Imaging System?

The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Arthrex SynergyID Endoscopic Imaging System?

The FDA product code for Arthrex SynergyID Endoscopic Imaging System is GCJ.

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Official Source

View on FDA Database →

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

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