FDA 510(k) Applications Submitted by INTERBODY INNOVATIONS LLP
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K051371 | 05/26/2005 | INTERBODY INNOVATIONS CEMENT RESTRICTOR | INTERBODY INNOVATIONS LLP |
| K062992 | 10/02/2006 | SPINAL SPHERES | INTERBODY INNOVATIONS LLP |
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