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FDA 510(k)

INSTRUMENTS, GENERAL HAND & SURGERY

K-Number: K760311 · 1976-08-09

ApplicantDepuy, Inc.
Decision Date1976-08-09
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENTS, GENERAL HAND & SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1976-08-09 under 510(k) number K760311. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENTS, GENERAL HAND & SURGERY?

INSTRUMENTS, GENERAL HAND & SURGERY is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Depuy, Inc.. The 510(k) number is K760311.

When did INSTRUMENTS, GENERAL HAND & SURGERY receive FDA 510(k) clearance?

INSTRUMENTS, GENERAL HAND & SURGERY received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760311.

Who is the listed applicant for INSTRUMENTS, GENERAL HAND & SURGERY?

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 INSTRUMENTS, GENERAL HAND & SURGERY?

The FDA product code for INSTRUMENTS, GENERAL HAND & SURGERY is FSM.

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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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