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FDA 510(k)

TOTAL HIP SYSTEM, HARRIS HD2

K-Number: K780317 · 1978-03-06

ApplicantHowmedica Corp.
Decision Date1978-03-06
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TOTAL HIP SYSTEM, HARRIS HD2 is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1978-03-06 under 510(k) number K780317. 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 TOTAL HIP SYSTEM, HARRIS HD2?

TOTAL HIP SYSTEM, HARRIS HD2 is a medical device that received FDA 510(k) clearance on 1978-03-06. The listed applicant is Howmedica Corp.. The 510(k) number is K780317.

When did TOTAL HIP SYSTEM, HARRIS HD2 receive FDA 510(k) clearance?

TOTAL HIP SYSTEM, HARRIS HD2 received FDA 510(k) clearance on 1978-03-06, under 510(k) number K780317.

Who is the listed applicant for TOTAL HIP SYSTEM, HARRIS HD2?

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 TOTAL HIP SYSTEM, HARRIS HD2?

The FDA product code for TOTAL HIP SYSTEM, HARRIS HD2 is JDI.

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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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