FDA 510(k) Applications Submitted by OSTEOGENICS CO.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K972278 | 06/18/1997 | CYTOPLAST REGENTEX TITANIUM 250 | OSTEOGENICS CO. |
| K964342 | 10/31/1996 | CYTOPLAST GBR | OSTEOGENICS CO. |
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