510(k) K071879

ZIMMER DTO IMPLANT by Zimmer Spine, Inc. — Product Code NQP

Clearance Details

Decision
SESU ()
Decision Date
October 5, 2007
Date Received
July 9, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Posterior Metal/Polymer Spinal System, Fusion
Device Class
Class II
Regulation Number
888.3070
Review Panel
OR
Submission Type

This device is a posterior spinal system that contains polymer and metal components. This spinal system is to be used with bone graft and is an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine.