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 a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2021-07-22 under approval 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. It is manufactured by Arthrex, Inc.. The 510(k) number is K202582.
When was Arthrex SynergyID Endoscopic Imaging System approved by the FDA?
Arthrex SynergyID Endoscopic Imaging System received FDA 510(k) clearance on 2021-07-22, under approval number K202582.
What company makes Arthrex SynergyID Endoscopic Imaging System?
Arthrex SynergyID Endoscopic Imaging System is manufactured by Arthrex, Inc..
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.