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FDA 510(k)

HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM

K-Number: K954559 · 1996-07-12

ApplicantHowmedica Corp.
Decision Date1996-07-12
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1996-07-12 under 510(k) number K954559. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM?

HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-12. The listed applicant is Howmedica Corp.. The 510(k) number is K954559.

When did HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM receive FDA 510(k) clearance?

HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM received FDA 510(k) clearance on 1996-07-12, under 510(k) number K954559.

Who is the listed applicant for HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM?

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 HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM?

The FDA product code for HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM is HSD.

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Other records listing Howmedica Corp. as applicant

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Related Devices (Code: HSD)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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