FDA 510(k)

TITANIUM M.E. MULLER TYPE TOTAL HIP

K-Number: K830356 · 1983-03-09

Decision Date1983-03-09

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

TITANIUM M.E. MULLER TYPE TOTAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Mannheim Corp.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830356. 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 TITANIUM M.E. MULLER TYPE TOTAL HIP?

TITANIUM M.E. MULLER TYPE TOTAL HIP is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K830356.

When did TITANIUM M.E. MULLER TYPE TOTAL HIP receive FDA 510(k) clearance?

TITANIUM M.E. MULLER TYPE TOTAL HIP received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830356.

Who is the listed applicant for TITANIUM M.E. MULLER TYPE TOTAL HIP?

The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM M.E. MULLER TYPE TOTAL HIP?

The FDA product code for TITANIUM M.E. MULLER TYPE TOTAL HIP 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.