FDA 510(k) Applications Submitted by N SPINE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072685 | 09/21/2007 | NGARDE SYSTEM | N SPINE, INC. |
| K061774 | 06/23/2006 | NFIX II PEDICLE SCREW SYSTEM | N SPINE, INC. |
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