510(k) K073347

DYNESYS TOP-LOADING SPINAL SYSTEM by Zimmer Spine, Inc. — Product Code NQP

K073347 is an FDA 510(k) premarket notification submitted by Zimmer Spine, Inc. for the device "DYNESYS TOP-LOADING SPINAL SYSTEM". The FDA issued a decision of SESU on February 8, 2008. The device falls under product code NQP (Posterior Metal/Polymer Spinal System, Fusion), a Class II device regulated under 21 CFR 888.3070. Zimmer Spine, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESU ()
Decision Date
February 8, 2008
Date Received
November 29, 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.