meddevicedb.com FDA Device Reference

ULTIMA*UNIPOLAR HEAD AND ADAPTER SLEEVES

K965156 Class II Traditional
Decision Date
1997-01-24
Sponsor / Applicant
Johnson & Johnson Professionals, Inc.

Technical Specification

510(k) Submission ID K965156
Product Code KWL
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3360
Decision Date 1997-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTIMA*UNIPOLAR HEAD AND ADAPTER SLEEVES received FDA 510(k) clearance under submission number K965156, 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 1997-01-24.

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.