Arthrex Virtual Implant Positioning (VIP) System— 510(k) K222007

Name: FDA 510(k) clearance K222007
Creator: U.S. Food and Drug Administration
Published: 2023-03-08

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K222007 for Arthrex Virtual Implant Positioning (VIP) System, Substantially Equivalent on 2023-03-08. Applicant: Arthrex, Inc.. Device class: 2.

Clearance details

Applicant: Arthrex, Inc.
Product code: Code QHE
Device class: Class 2
Regulation: 21 CFR 888.3660
Advisory panel: Orthopedic
Date received: 2022-07-07
Decision date: 2023-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

Download summary PDF View on FDA.gov ↗

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