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FDA 510(k)

TITANIUM MULLER TOTAL HIP

K-Number: K780357 · 1978-04-05

ApplicantBiomet, Inc.
Decision Date1978-04-05
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TITANIUM MULLER TOTAL HIP is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1978-04-05 under 510(k) number K780357. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TITANIUM MULLER TOTAL HIP?

TITANIUM MULLER TOTAL HIP is a medical device that received FDA 510(k) clearance on 1978-04-05. The listed applicant is Biomet, Inc.. The 510(k) number is K780357.

When did TITANIUM MULLER TOTAL HIP receive FDA 510(k) clearance?

TITANIUM MULLER TOTAL HIP received FDA 510(k) clearance on 1978-04-05, under 510(k) number K780357.

Who is the listed applicant for TITANIUM MULLER TOTAL HIP?

The FDA 510(k) record lists Biomet, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TITANIUM MULLER TOTAL HIP?

The FDA product code for TITANIUM MULLER TOTAL HIP is JDG.

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Other records listing Biomet, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253434OSSTM Orthopedic Salvage SystemK251270Taperloc® Complete Hip StemK241014Biomet Kirschner Wires (K-Wires)K222760StageOne™ Select Hip Cement Spacer MoldsK221968StageOne™ Shoulder Cement Spacer MoldsK213287StageOne Knee Cement Spacer Molds

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Related Devices (Code: JDG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.K193546Distal CentralizersBiomet, Inc.K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker OrthopaedicsK001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast CompanyK992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USAK962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, Inc.

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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