| Proprietary Device Name: | MULTIPLE: PRO OSTEON 200R, PRO OSTEON 500R & BONEPLAST |
| Common Generic Device Name: | BONE GRAFT SUBSTITUTE OR VOID FILLER |
| Classification Name: | FILLER, CALCIUM SULFATE PREFORMED PELLETS |
| FDA Regulation Number: | 888.3045 |
| Product Differentiation: | |
| Product Website: |