FDA 510(k) Applications Submitted by SPINECRAFT, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062513 | 08/28/2006 | APEX SPINE SYSTEM | SPINECRAFT, INC. |
| K092825 | 09/11/2009 | APEX SPINE SYSTEM 5.50 MM TITANIUM ROD & POLYAXIAL SCREW WASHER | SPINECRAFT, INC. |
| K062496 | 08/25/2006 | OSTEOPORE TCP | SPINECRAFT, INC. |
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