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PERIMETER C SPINAL SYSTEM

K132584 Class II Traditional
Decision Date
2013-12-04
Sponsor / Applicant
Medtronic Sofamor Danek USA, Inc.

Technical Specification

510(k) Submission ID K132584
Product Code ODP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3080
Decision Date 2013-12-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERIMETER C SPINAL SYSTEM received FDA 510(k) clearance under submission number K132584, sponsored by Medtronic Sofamor Danek USA, 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 2013-12-04.

Classification & Regulation

This clearance is catalogued under FDA product code ODP and 21 CFR 888.3080, within the Orthopedic review panel as a Class II device.