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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 the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. It received FDA 510(k) clearance on 2021-06-04 under 510(k) 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. The listed applicant is Howmedica Osteonics Corp., Dba Stryker Orthopaedics. The 510(k) number is K211303.

When did Avon Patello-femoral Joint Prosthesis receive FDA 510(k) clearance?

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

Who is the listed applicant for Avon Patello-femoral Joint Prosthesis?

The FDA 510(k) record lists Howmedica Osteonics Corp., Dba Stryker Orthopaedics as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Howmedica Osteonics Corp., Dba Stryker Orthopaedics as applicant

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Related Devices (Code: KRR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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