FDA 510(k) Applications Submitted by CEREMED INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K041363 | 05/21/2004 | AOC BONE WAX | CEREMED INC. |
| K091636 | 06/04/2009 | OSTENE CT, AOC CT, OSTEOTENE, CERETENE | CEREMED INC. |
| K070093 | 01/10/2007 | OSTENE, AOC, OSTEOTENE, CERETENE, CEREPOR, APTENE, APATENE, ACTIPASTE | CEREMED INC. |
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