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SPIDER CERVICAL PLATING (SCP) SYSTEM

K052292 Class II Traditional
Decision Date
2005-10-21
Sponsor / Applicant
X-Spine Systems, Inc.

Technical Specification

510(k) Submission ID K052292
Product Code KWQ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3060
Decision Date 2005-10-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPIDER CERVICAL PLATING (SCP) SYSTEM received FDA 510(k) clearance under submission number K052292, sponsored by X-Spine Systems, 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 2005-10-21.

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.