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FDA 510(k)

TOTAL HIP, LORD MADREPORIC

K-Number: K780330 · 1978-05-12

ApplicantHowmedica Corp.
Decision Date1978-05-12
Product CodeKWA
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TOTAL HIP, LORD MADREPORIC is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1978-05-12 under 510(k) number K780330. The device is classified under product code KWA. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOTAL HIP, LORD MADREPORIC?

TOTAL HIP, LORD MADREPORIC is a medical device that received FDA 510(k) clearance on 1978-05-12. The listed applicant is Howmedica Corp.. The 510(k) number is K780330.

When did TOTAL HIP, LORD MADREPORIC receive FDA 510(k) clearance?

TOTAL HIP, LORD MADREPORIC received FDA 510(k) clearance on 1978-05-12, under 510(k) number K780330.

Who is the listed applicant for TOTAL HIP, LORD MADREPORIC?

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, LORD MADREPORIC?

The FDA product code for TOTAL HIP, LORD MADREPORIC is KWA.

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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: KWA)

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.

K122778PROFEMUR Z REVISION HIP STEMWrightmedicaltechnologyincK121544DYNASTY BIOFOAM SHELLWrightmedicaltechnologyincK113271METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONSBiomet Manufacturing, Inc.K113322CONSERVE THIN SHELLWrightmedicaltechnologyincK112080PRESERVE HIP STEMWrightmedicaltechnologyincK112150PROFEMUR GLADIATOR HA HIP STEMWrightmedicaltechnologyinc

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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