Skeletal Kinetics, LLC
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162864 | OsteoVation Impact | GXP | 2017-01-13 | View |
| 510(k) | K120354 | BETA-TCP GRANULES | MQV | 2013-03-21 | View |
| 510(k) | K112383 | CALLOS PROMODEL BONE VOID FILLER, SKAFFOLD MP (MACRO POROUS) BONE VOID FILLER | MQV | 2012-02-07 | View |
| 510(k) | K111538 | SKAFFOLD CIS | MTJ | 2011-10-25 | View |
| 510(k) | K100986 | CALLOS BONE VOID FILLER, SKAFFOLD NEXT GENERATION BONE VOID FILLER, OSTEO VATION | MQV | 2010-07-20 | View |
| 510(k) | K051784 | OSTEOVATION CMF BONE VOID FILLER | GXP | 2005-07-20 | View |
| 510(k) | K051123 | CALLOS IMPACT AND INJECT BONE VOID FILLER | MQV | 2005-06-03 | View |
| 510(k) | K042072 | CALLOS CMF BONE VOID FILLER | GXP | 2004-09-16 | View |
| 510(k) | K030554 | CALLOS | MQV | 2003-05-20 | View |
No matching devices.
Advertisement