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FDA 510(k)

TITAN TOTAL HIP DEVICE

K-Number: K905298 · 1991-06-17

ApplicantDr. Jean-Marc Guichet
Decision Date1991-06-17
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITAN TOTAL HIP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Jean-Marc Guichet. It received FDA 510(k) clearance on 1991-06-17 under 510(k) number K905298. 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 TITAN TOTAL HIP DEVICE?

TITAN TOTAL HIP DEVICE is a medical device that received FDA 510(k) clearance on 1991-06-17. The listed applicant is Dr. Jean-Marc Guichet. The 510(k) number is K905298.

When did TITAN TOTAL HIP DEVICE receive FDA 510(k) clearance?

TITAN TOTAL HIP DEVICE received FDA 510(k) clearance on 1991-06-17, under 510(k) number K905298.

Who is the listed applicant for TITAN TOTAL HIP DEVICE?

The FDA 510(k) record lists Dr. Jean-Marc Guichet as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITAN TOTAL HIP DEVICE?

The FDA product code for TITAN TOTAL HIP DEVICE 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.

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