meddevicedb.com FDA Device Reference

CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5

K953792 Class II Traditional
Decision Date
1995-11-06
Sponsor / Applicant
U.S. Medical Products, Inc.

Technical Specification

510(k) Submission ID K953792
Product Code LZO
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3353
Decision Date 1995-11-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONSENSUS ZIRCONIA HEAD SIZE -3.5, 0, +5 received FDA 510(k) clearance under submission number K953792, sponsored by U.S. Medical Products, 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 1995-11-06.

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.