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PROSTHESIS, VIDAL TOTAL HIP

K770472 Class III Traditional
Decision Date
1977-03-17
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K770472
Product Code JDL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3320
Decision Date 1977-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROSTHESIS, VIDAL TOTAL HIP received FDA 510(k) clearance under submission number K770472, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1977-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code JDL and 21 CFR 888.3320, within the Orthopedic review panel as a Class III device.