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FDA 510(k)

HOMEDICA CEMENTED ACETABULAR COMPONENT 6262

K-Number: K851565 · 1985-07-19

ApplicantHowmedica Corp.
Decision Date1985-07-19
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HOMEDICA CEMENTED ACETABULAR COMPONENT 6262 is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1985-07-19 under 510(k) number K851565. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOMEDICA CEMENTED ACETABULAR COMPONENT 6262?

HOMEDICA CEMENTED ACETABULAR COMPONENT 6262 is a medical device that received FDA 510(k) clearance on 1985-07-19. The listed applicant is Howmedica Corp.. The 510(k) number is K851565.

When did HOMEDICA CEMENTED ACETABULAR COMPONENT 6262 receive FDA 510(k) clearance?

HOMEDICA CEMENTED ACETABULAR COMPONENT 6262 received FDA 510(k) clearance on 1985-07-19, under 510(k) number K851565.

Who is the listed applicant for HOMEDICA CEMENTED ACETABULAR COMPONENT 6262?

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

What is the FDA product code for HOMEDICA CEMENTED ACETABULAR COMPONENT 6262?

The FDA product code for HOMEDICA CEMENTED ACETABULAR COMPONENT 6262 is DXQ.

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Related Devices (Code: DXQ)

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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