Arthrex Synergy Vision Endoscopic Imaging System
K-Number: K241361 · 2024-07-25
ApplicantArthrex, Inc.
Decision Date2024-07-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Arthrex Synergy Vision Endoscopic Imaging System is a medical device manufactured by Arthrex, Inc.. It received FDA 510(k) clearance on 2024-07-25 under approval number K241361. 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 Synergy Vision Endoscopic Imaging System?
Arthrex Synergy Vision Endoscopic Imaging System is a medical device that received FDA 510(k) clearance on 2024-07-25. It is manufactured by Arthrex, Inc.. The 510(k) number is K241361.
When was Arthrex Synergy Vision Endoscopic Imaging System approved by the FDA?
Arthrex Synergy Vision Endoscopic Imaging System received FDA 510(k) clearance on 2024-07-25, under approval number K241361.
What company makes Arthrex Synergy Vision Endoscopic Imaging System?
Arthrex Synergy Vision Endoscopic Imaging System is manufactured by Arthrex, Inc..
What is the FDA product code for Arthrex Synergy Vision Endoscopic Imaging System?
The FDA product code for Arthrex Synergy Vision 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.