510(k) K073347
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.