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ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM

K951000 Class II Traditional
Decision Date
1995-04-14
Sponsor / Applicant
Joint Medical Products Corp.

Technical Specification

510(k) Submission ID K951000
Product Code LPH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3358
Decision Date 1995-04-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZTT I AND II ACETABULAR CUP OF THE S-ROM TOTAL HIP SYSTEM received FDA 510(k) clearance under submission number K951000, sponsored by Joint Medical Products 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 1995-04-14.

Classification & Regulation

This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.