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FDA 510(k)

AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT

K-Number: K041160 · 2004-05-27

ApplicantHowmedica Osteonics Corp.
Decision Date2004-05-27
Product CodeKRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2004-05-27 under 510(k) number K041160. 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 EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT?

AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT is a medical device that received FDA 510(k) clearance on 2004-05-27. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K041160.

When did AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT receive FDA 510(k) clearance?

AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT received FDA 510(k) clearance on 2004-05-27, under 510(k) number K041160.

Who is the listed applicant for AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT?

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

What is the FDA product code for AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT?

The FDA product code for AVON EXTRA-SMALL PATELLO-FEMORAL REPLACEMENT is KRR.

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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.

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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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