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ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600

K072183 Class II Special
Decision Date
2007-09-05
Sponsor / Applicant
Zimmer Spine, Inc.

Technical Specification

510(k) Submission ID K072183
Product Code NKB
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3070
Decision Date 2007-09-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ST360 SPINAL FIXATION SYSTEM, MODEL 07.0029-7500.5600 received FDA 510(k) clearance under submission number K072183, sponsored by Zimmer Spine, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2007-09-05.

Classification & Regulation

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