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ZODIAC DYNAMO SEMI-RIGID SPINAL SYSTEM

K072081 Class II Traditional
Decision Date
2007-10-24
Sponsor / Applicant
Alphatec Spine, Inc.

Technical Specification

510(k) Submission ID K072081
Product Code KWP
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3050
Decision Date 2007-10-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZODIAC DYNAMO SEMI-RIGID SPINAL SYSTEM received FDA 510(k) clearance under submission number K072081, sponsored by Alphatec Spine, 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 2007-10-24.

Classification & Regulation

This clearance is catalogued under FDA product code KWP and 21 CFR 888.3050, within the Orthopedic review panel as a Class II device.