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EVOLUTION HIP SYSTEM

K896105 Class II Traditional
Decision Date
1989-12-29
Sponsor / Applicant
Dow Corning Wright

Technical Specification

510(k) Submission ID K896105
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1989-12-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVOLUTION HIP SYSTEM received FDA 510(k) clearance under submission number K896105, sponsored by Dow Corning Wright. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1989-12-29.

Classification & Regulation

This clearance is catalogued under FDA product code KWL and 21 CFR 888.3360, within the Orthopedic review panel as a Class II device.