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CONTOUR II SPINAL SYSTEM

K053070 Class II Traditional
Decision Date
2006-02-13
Sponsor / Applicant
Altiva Corp.

Technical Specification

510(k) Submission ID K053070
Product Code MNH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2006-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTOUR II SPINAL SYSTEM received FDA 510(k) clearance under submission number K053070, sponsored by Altiva Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2006-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code MNH and 21 CFR 888.3070, within the Orthopedic review panel as a Class II device.