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FDA 510(k)

PROSTHESIS, TOTAL HIP-TEST CUP

K-Number: K760108 · 1976-07-20

ApplicantOrthopedic Equipment Co., Inc.
Decision Date1976-07-20
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, TOTAL HIP-TEST CUP is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760108. 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 PROSTHESIS, TOTAL HIP-TEST CUP?

PROSTHESIS, TOTAL HIP-TEST CUP is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K760108.

When did PROSTHESIS, TOTAL HIP-TEST CUP receive FDA 510(k) clearance?

PROSTHESIS, TOTAL HIP-TEST CUP received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760108.

Who is the listed applicant for PROSTHESIS, TOTAL HIP-TEST CUP?

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

What is the FDA product code for PROSTHESIS, TOTAL HIP-TEST CUP?

The FDA product code for PROSTHESIS, TOTAL HIP-TEST CUP is JDG.

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Other records listing Orthopedic Equipment Co., 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.

K834035UNIVERSAL SELF-ALIGNING ACETABULAR COMK841189OEC/REZAIAN SPINAL FIXATORK800530SCHLEIN TRI-SURFACE ANKLEK781445SPREADERK790247TOURNIQUET TEST GAGEK790209FILTER SYSTEM, ALTNER DISPOSABLE

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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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