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SURGICAL INSTRUMENTS, ORTHOPEDIC

K760325 Class I Traditional
Decision Date
1976-08-03
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K760325
Product Code HTX
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4540
Decision Date 1976-08-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGICAL INSTRUMENTS, ORTHOPEDIC received FDA 510(k) clearance under submission number K760325, sponsored by Depuy, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1976-08-03.

Classification & Regulation

This clearance is catalogued under FDA product code HTX and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.