FDA 510(k)

HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE

K-Number: K934060 · 1995-08-18

Decision Date1995-08-18

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-08-18 under 510(k) number K934060. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE?

HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE is a medical device that received FDA 510(k) clearance on 1995-08-18. The listed applicant is Howmedica Corp.. The 510(k) number is K934060.

When did HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE receive FDA 510(k) clearance?

HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE received FDA 510(k) clearance on 1995-08-18, under 510(k) number K934060.

Who is the listed applicant for HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE?

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 HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE?

The FDA product code for HOWMEDICA(R) ACETABULAR COMP PACK/MANUF METH CHANGE is LPH.

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Other records listing Howmedica Corp. as applicant

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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.