Isotis NV
FDA 510(k) & PMA Approved Devices — 8 products
Advertisement
Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K061880 | ACCELI DBM FAMILY PRODUCTS, 0.5CC, 1CC, 2.5CC, 5CC, 10CC, 15CC, 30CC | MQV | 2007-08-15 | View |
| 510(k) | K060332 | ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY | NUN | 2006-03-29 | View |
| 510(k) | K060306 | ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY | NUN | 2006-03-27 | View |
| 510(k) | K031813 | OSSATURA DENTAL | LYC | 2004-08-20 | View |
| 510(k) | K041344 | OPEN BORE SYRINGE | FMF | 2004-07-16 | View |
| 510(k) | K030131 | OSSATURA BCP BONE VOID FILLER | MQV | 2003-05-20 | View |
| 510(k) | K010840 | SYNPLUG | LZN | 2001-04-20 | View |
| 510(k) | K000587 | SHUTTLE STOP | LZN | 2000-05-04 | View |
No matching devices.
Advertisement