meddevicedb.com FDA Device Reference

S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEAD

K973307 Class II Traditional
Decision Date
1997-11-20
Sponsor / Applicant
Johnson & Johnson Professionals, Inc.

Technical Specification

510(k) Submission ID K973307
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1997-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S-ROM ZIRCONIA CERAMIC FEMORAL HIP HEAD received FDA 510(k) clearance under submission number K973307, sponsored by Johnson & Johnson Professionals, 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 1997-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code LZO and 21 CFR 888.3353, within the Orthopedic review panel as a Class II device.