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PREMIER ANTERIOR CERVICAL PLATE SYSTEM

K992110 Class II Traditional
Decision Date
1999-09-14
Sponsor / Applicant
Sofamor Danek USA

Technical Specification

510(k) Submission ID K992110
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 1999-09-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PREMIER ANTERIOR CERVICAL PLATE SYSTEM received FDA 510(k) clearance under submission number K992110, sponsored by Sofamor Danek USA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1999-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code KWQ and 21 CFR 888.3060, within the Orthopedic review panel as a Class II device.