FDA 510(k) Applications Submitted by OSTEOTECH INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K082615 | 09/09/2008 | GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES | OSTEOTECH INC |
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