FDA 510(k)

VITALOCK SOLID BACKED ACETABULAR SHELL

K-Number: K952397 · 1995-07-21

Decision Date1995-07-21

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

VITALOCK SOLID BACKED ACETABULAR SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-07-21 under 510(k) number K952397. 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 VITALOCK SOLID BACKED ACETABULAR SHELL?

VITALOCK SOLID BACKED ACETABULAR SHELL is a medical device that received FDA 510(k) clearance on 1995-07-21. The listed applicant is Howmedica Corp.. The 510(k) number is K952397.

When did VITALOCK SOLID BACKED ACETABULAR SHELL receive FDA 510(k) clearance?

VITALOCK SOLID BACKED ACETABULAR SHELL received FDA 510(k) clearance on 1995-07-21, under 510(k) number K952397.

Who is the listed applicant for VITALOCK SOLID BACKED ACETABULAR SHELL?

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 VITALOCK SOLID BACKED ACETABULAR SHELL?

The FDA product code for VITALOCK SOLID BACKED ACETABULAR SHELL is LPH.

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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.