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DEPUY MOTECH PEAK FIXATION SYSTEM

K963350 Class II Traditional
Decision Date
1996-11-14
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K963350
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1996-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DEPUY MOTECH PEAK FIXATION SYSTEM received FDA 510(k) clearance under submission number K963350, 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 1996-11-14.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.