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FDA 510(k)

LAGRANGE LETOURNEL TOTAL HIP FEMORAL

K-Number: K770473 · 1977-03-17

ApplicantHowmedica Corp.
Decision Date1977-03-17
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LAGRANGE LETOURNEL TOTAL HIP FEMORAL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1977-03-17 under 510(k) number K770473. 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 LAGRANGE LETOURNEL TOTAL HIP FEMORAL?

LAGRANGE LETOURNEL TOTAL HIP FEMORAL is a medical device that received FDA 510(k) clearance on 1977-03-17. The listed applicant is Howmedica Corp.. The 510(k) number is K770473.

When did LAGRANGE LETOURNEL TOTAL HIP FEMORAL receive FDA 510(k) clearance?

LAGRANGE LETOURNEL TOTAL HIP FEMORAL received FDA 510(k) clearance on 1977-03-17, under 510(k) number K770473.

Who is the listed applicant for LAGRANGE LETOURNEL TOTAL HIP FEMORAL?

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 LAGRANGE LETOURNEL TOTAL HIP FEMORAL?

The FDA product code for LAGRANGE LETOURNEL TOTAL HIP FEMORAL is JDG.

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Other records listing Howmedica Corp. 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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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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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