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UNIVERSAL SPINAL ANTERIOR LOCKING PLATE SYSTEM

K062686 Class II Special
Decision Date
2006-10-05
Sponsor / Applicant
Advanced Spine Technology, Inc.

Technical Specification

510(k) Submission ID K062686
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2006-10-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIVERSAL SPINAL ANTERIOR LOCKING PLATE SYSTEM received FDA 510(k) clearance under submission number K062686, sponsored by Advanced Spine Technology, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-10-05.

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.