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SPINAL CONCEPTS, INC., UNIVERSAL BONE PLATE SYSTEM II

K973586 Class II Traditional
Decision Date
1997-11-07
Sponsor / Applicant
Spinal Concepts, Inc.

Technical Specification

510(k) Submission ID K973586
Product Code HWC
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 1997-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPINAL CONCEPTS, INC., UNIVERSAL BONE PLATE SYSTEM II received FDA 510(k) clearance under submission number K973586, sponsored by Spinal Concepts, 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 1997-11-07.

Classification & Regulation

This clearance is catalogued under FDA product code HWC and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.