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FDA 510(k)

PARTNERSHIP CALCAR FEMORAL COMPONENTS

K-Number: K980239 · 1998-04-16

ApplicantHowmedica, Inc.
Decision Date1998-04-16
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PARTNERSHIP CALCAR FEMORAL COMPONENTS is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Inc.. It received FDA 510(k) clearance on 1998-04-16 under 510(k) number K980239. 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 PARTNERSHIP CALCAR FEMORAL COMPONENTS?

PARTNERSHIP CALCAR FEMORAL COMPONENTS is a medical device that received FDA 510(k) clearance on 1998-04-16. The listed applicant is Howmedica, Inc.. The 510(k) number is K980239.

When did PARTNERSHIP CALCAR FEMORAL COMPONENTS receive FDA 510(k) clearance?

PARTNERSHIP CALCAR FEMORAL COMPONENTS received FDA 510(k) clearance on 1998-04-16, under 510(k) number K980239.

Who is the listed applicant for PARTNERSHIP CALCAR FEMORAL COMPONENTS?

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

What is the FDA product code for PARTNERSHIP CALCAR FEMORAL COMPONENTS?

The FDA product code for PARTNERSHIP CALCAR FEMORAL COMPONENTS is LZO.

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Other records listing Howmedica, Inc. as applicant

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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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