Teknimed, S.A.
FDA 510(k) & PMA Approved Devices — 11 products
Advertisement
Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K103433 | F20 | NDN | 2011-01-03 | View |
| 510(k) | K090435 | VERTECEM | NDN | 2009-12-21 | View |
| 510(k) | K083005 | NANGEL | LYC | 2009-03-04 | View |
| 510(k) | K080873 | OPACITY + BONE CEMENT | NDN | 2008-08-28 | View |
| 510(k) | K062102 | ODONCER | LYC | 2007-04-16 | View |
| 510(k) | K043593 | SPINE-FIX BIOMIMETIC BONE CEMENT | NDN | 2006-03-17 | View |
| 510(k) | K042911 | CEMENTEK LV | MQV | 2004-12-27 | View |
| 510(k) | K041493 | CEMENTEK | MQV | 2004-08-19 | View |
| 510(k) | K040669 | CERAFORM BONE VOID FILLER | MQV | 2004-05-03 | View |
| 510(k) | K031826 | TRIHA + | MQV | 2003-11-28 | View |
| 510(k) | K032685 | CEMSTOP CEMENT RESTRICTOR | LZN | 2003-11-26 | View |
No matching devices.
Advertisement