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FDA 510(k)

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT

K-Number: K013982 · 2002-05-21

ApplicantKinamed, Inc.
Decision Date2002-05-21
Product CodeKRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT is the device name listed in this FDA 510(k) record. The listed applicant is Kinamed, Inc.. It received FDA 510(k) clearance on 2002-05-21 under 510(k) number K013982. 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 KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT?

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT is a medical device that received FDA 510(k) clearance on 2002-05-21. The listed applicant is Kinamed, Inc.. The 510(k) number is K013982.

When did KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT receive FDA 510(k) clearance?

KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT received FDA 510(k) clearance on 2002-05-21, under 510(k) number K013982.

Who is the listed applicant for KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT?

The FDA 510(k) record lists Kinamed, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT?

The FDA product code for KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT is KRR.

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Other records listing Kinamed, Inc. 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.K211303Avon Patello-femoral Joint ProsthesisHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK200122MOTO 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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