Overture Orthopaedics Patellofemoral System— 510(k) K231253

Name: FDA 510(k) clearance K231253
Creator: U.S. Food and Drug Administration
Published: 2023-07-07

Substantially Equivalent

Overture Resurfacing, Inc.

FDA 510(k) clearance K231253 for Overture Orthopaedics Patellofemoral System, Substantially Equivalent on 2023-07-07. Applicant: Overture Resurfacing, Inc.. Device class: 2.

Clearance details

Applicant: Overture Resurfacing, Inc.
Product code: Code KRR
Device class: Class 2
Regulation: 21 CFR 888.3540
Advisory panel: Orthopedic
Date received: 2023-05-01
Decision date: 2023-07-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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