FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Arthrex Synergy Vision Endoscopic Imaging System

K Number: K250728 · Decision May 5, 2025
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
1391
Applicant Total
36
Review Days
55

Basic Information

Device Name
Arthrex Synergy Vision Endoscopic Imaging System
K Number
K250728
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrex, Inc.
Date Received
March 11, 2025
Decision Date
May 5, 2025
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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