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FDA 510(k)

PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL

K-Number: K770856 · 1977-05-23

ApplicantDepuy, Inc.
Decision Date1977-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1977-05-23 under 510(k) number K770856. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL?

PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL is a medical device that received FDA 510(k) clearance on 1977-05-23. The listed applicant is Depuy, Inc.. The 510(k) number is K770856.

When did PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL receive FDA 510(k) clearance?

PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL received FDA 510(k) clearance on 1977-05-23, under 510(k) number K770856.

Who is the listed applicant for PROSTHESIS, TRAPEZIUM & TRAPEZIUM TRIAL?

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

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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