FDA 510(k) Applications Submitted by IBALANCE MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K092381 | 08/05/2009 | IBALANCE AKRFX MEDIAL OPENING WEDGE TIBIAL SYSTEM, IFX MEDIAL PEEK IMPLANT AND ANCHOR, AKRFX INSTRUMENTATION | IBALANCE MEDICAL, INC. |
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