FDA 510(k)

CDH HIP SYSTEM

K-Number: K922008 · 1992-07-30

ApplicantHowmedica, Pfizer Medical Technology Group

Decision Date1992-07-30

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CDH HIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica, Pfizer Medical Technology Group. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K922008. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDH HIP SYSTEM?

CDH HIP SYSTEM is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Howmedica, Pfizer Medical Technology Group. The 510(k) number is K922008.

When did CDH HIP SYSTEM receive FDA 510(k) clearance?

CDH HIP SYSTEM received FDA 510(k) clearance on 1992-07-30, under 510(k) number K922008.

Who is the listed applicant for CDH HIP SYSTEM?

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

What is the FDA product code for CDH HIP SYSTEM?

The FDA product code for CDH HIP SYSTEM is JDI.

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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.