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FDA 510(k)

PROSTHESIS, HIP, CATHCART, SCHILLER MOD.

K-Number: K780773 · 1978-06-22

ApplicantDepuy, Inc.
Decision Date1978-06-22
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, HIP, CATHCART, SCHILLER MOD. is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1978-06-22 under 510(k) number K780773. 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, HIP, CATHCART, SCHILLER MOD.?

PROSTHESIS, HIP, CATHCART, SCHILLER MOD. is a medical device that received FDA 510(k) clearance on 1978-06-22. The listed applicant is Depuy, Inc.. The 510(k) number is K780773.

When did PROSTHESIS, HIP, CATHCART, SCHILLER MOD. receive FDA 510(k) clearance?

PROSTHESIS, HIP, CATHCART, SCHILLER MOD. received FDA 510(k) clearance on 1978-06-22, under 510(k) number K780773.

Who is the listed applicant for PROSTHESIS, HIP, CATHCART, SCHILLER MOD.?

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

What is the FDA product code for PROSTHESIS, HIP, CATHCART, SCHILLER MOD.?

The FDA product code for PROSTHESIS, HIP, CATHCART, SCHILLER MOD. is JDG.

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Other records listing Depuy, Inc. as applicant

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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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