FDA 510(k) Applications Submitted by CAROL EMERSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090767 | 03/23/2009 | PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER | INTERVENTIONAL SPINE, INC. |
| K082795 | 09/23/2008 | SINGLE USE PERPOS PLS SYSTEM, 4.5 BONE-LOK PLS IMPLANT | INTERVENTIONAL SPINE, INC. |
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