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MODIFIED SYNATOMIC VARIABLE FIT TIBIAL PLATEAU

K860133 Class II Traditional
Decision Date
1986-03-10
Sponsor / Applicant
Depuy, Inc.

Technical Specification

510(k) Submission ID K860133
Product Code HRY
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3530
Decision Date 1986-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED SYNATOMIC VARIABLE FIT TIBIAL PLATEAU received FDA 510(k) clearance under submission number K860133, 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 1986-03-10.

Classification & Regulation

This clearance is catalogued under FDA product code HRY and 21 CFR 888.3530, within the Orthopedic review panel as a Class II device.