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FDA 510(k)

Avon Patello-femoral Joint Prosthesis

K-Number: K211303 · 2021-06-04

ApplicantHowmedica Osteonics Corp., Dba Stryker Orthopaedics
Decision Date2021-06-04
Product CodeKRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Avon Patello-femoral Joint Prosthesis is a medical device manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2021-06-04 under approval number K211303. The device is classified under product code KRR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Avon Patello-femoral Joint Prosthesis?

Avon Patello-femoral Joint Prosthesis is a medical device that received FDA 510(k) clearance on 2021-06-04. It is manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K211303.

When was Avon Patello-femoral Joint Prosthesis approved by the FDA?

Avon Patello-femoral Joint Prosthesis received FDA 510(k) clearance on 2021-06-04, under approval number K211303.

What company makes Avon Patello-femoral Joint Prosthesis?

Avon Patello-femoral Joint Prosthesis is manufactured by Howmedica Osteonics Corp., Dba Stryker Orthopaedics.

What is the FDA product code for Avon Patello-femoral Joint Prosthesis?

The FDA product code for Avon Patello-femoral Joint Prosthesis is KRR.

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Other Devices by Howmedica Osteonics Corp., Dba Stryker Orthopaedics

K202016Dall-Miles® Cable System K201343Triathlon Total KneeSystem K213129Restoration Modular 115mm Conical Distal Stem K222632UHR Bipolar Implants, Restoration GAP II Implants K220376Acetabular Dome Hole Plug K212187Restoration® Modular Hip System

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Related Devices (Code: KRR)

K160461Arthrex iBalance BiCompartmental Arthroplasty SystemArthrex, Inc. K181280Patello-Femoral Wave (Kahuna) Arthroplasty SystemArthrosurface, Inc. K200122MOTO PFJ SystemMedacta International S.A. K221048Episealer Patellofemoral SystemEpisurf Medical, Inc. K231253Overture Orthopaedics Patellofemoral SystemOverture Resurfacing, Inc.

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.

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