meddevicedb.com FDA Device Reference

UNIVERSAL CLAMP SPINAL FIXATION SYSTEM

K110348 Class II Traditional
Decision Date
2011-08-11
Sponsor / Applicant
Zimmer Spine

Technical Specification

510(k) Submission ID K110348
Product Code OWI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3010
Decision Date 2011-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIVERSAL CLAMP SPINAL FIXATION SYSTEM received FDA 510(k) clearance under submission number K110348, sponsored by Zimmer Spine. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2011-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code OWI and 21 CFR 888.3010, within the Orthopedic review panel as a Class II device.