FDA 510(k) Applications Submitted by MR. JOHN PARRY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150643 | 03/12/2015 | Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti | CENTINEL SPINE, INC. |
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