meddevicedb.com FDA Device Reference

OMEGA+ COMPRESSION SCREW SYSTEM

K955306 Class II Traditional
Decision Date
1996-04-10
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K955306
Product Code KTT
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3030
Decision Date 1996-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OMEGA+ COMPRESSION SCREW SYSTEM received FDA 510(k) clearance under submission number K955306, 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 1996-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code KTT and 21 CFR 888.3030, within the Orthopedic review panel as a Class II device.