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FDA 510(k)

ACCOLADE C FEMORAL STEMS

K-Number: K022555 · 2002-08-26

Decision Date2002-08-26
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACCOLADE C FEMORAL STEMS 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 2002-08-26 under 510(k) number K022555. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCOLADE C FEMORAL STEMS?

ACCOLADE C FEMORAL STEMS is a medical device that received FDA 510(k) clearance on 2002-08-26. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K022555.

When did ACCOLADE C FEMORAL STEMS receive FDA 510(k) clearance?

ACCOLADE C FEMORAL STEMS received FDA 510(k) clearance on 2002-08-26, under 510(k) number K022555.

Who is the listed applicant for ACCOLADE C FEMORAL STEMS?

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 ACCOLADE C FEMORAL STEMS?

The FDA product code for ACCOLADE C FEMORAL STEMS is LZO.

Related Clinical Trials

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.

Other records listing Howmedica Osteonics Corp. as applicant

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.

View all 288 devices →

Related Devices (Code: LZO)

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.

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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