FDA 510(k) Applications Submitted by SPECIALTY SPINE PRODUCTS, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060118 | 01/17/2006 | SSP PEDICLE SCREW SYSTEM | SPECIALTY SPINE PRODUCTS, LLC |
| K061578 | 06/07/2006 | SSP VERTEBRAL BODY REPLACEMENT | SPECIALTY SPINE PRODUCTS, LLC |
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