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FDA 510(k)

PARKE-DAVIS TOTAL HIP PROSTHESIS

K-Number: K791875 · 1979-10-04

ApplicantWarner-Lambert Co.
Decision Date1979-10-04
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PARKE-DAVIS TOTAL HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Warner-Lambert Co.. It received FDA 510(k) clearance on 1979-10-04 under 510(k) number K791875. 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 PARKE-DAVIS TOTAL HIP PROSTHESIS?

PARKE-DAVIS TOTAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1979-10-04. The listed applicant is Warner-Lambert Co.. The 510(k) number is K791875.

When did PARKE-DAVIS TOTAL HIP PROSTHESIS receive FDA 510(k) clearance?

PARKE-DAVIS TOTAL HIP PROSTHESIS received FDA 510(k) clearance on 1979-10-04, under 510(k) number K791875.

Who is the listed applicant for PARKE-DAVIS TOTAL HIP PROSTHESIS?

The FDA 510(k) record lists Warner-Lambert Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARKE-DAVIS TOTAL HIP PROSTHESIS?

The FDA product code for PARKE-DAVIS TOTAL HIP PROSTHESIS is DXQ.

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Related Devices (Code: DXQ)

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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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