Ebi, L.P.
FDA 510(k) & PMA Approved Devices — 95 products
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Total Devices95
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K100438 | POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM | NKB | 2010-06-23 | View |
| 510(k) | K100220 | POLARIS SPINAL SYSTEM | NKB | 2010-05-17 | View |
| 510(k) | K093880 | PEANUT GROWTH CONTROL PLATING SYSTEM | HRS | 2010-04-16 | View |
| 510(k) | K092574 | ESL SPINAL SYSTEM | MAX | 2010-02-04 | View |
| 510(k) | K093057 | BIOMET VISION FOOTRING SYSTEM | KTT | 2009-12-01 | View |
| 510(k) | K092336 | C-THRU SPINAL SYSTEM | MQP | 2009-10-15 | View |
| 510(k) | K091381 | IBEX SPINAL SYSTEM | MAX | 2009-08-07 | View |
| 510(k) | K090203 | 5.5 HELICAL FLANGE SPINAL SYSTEM, POLARIS COMPONENTS | NKB | 2009-07-30 | View |
| 510(k) | K090523 | POLARIS SPINAL SYSTEM | NKB | 2009-07-01 | View |
| 510(k) | K082406 | EXPANDABLE PEEK-OPTIMA IMPLANT | MAX | 2009-01-14 | View |
| 510(k) | K082187 | BIOMET ANTERIOR LUMBAR PLATE | KWQ | 2008-11-13 | View |
| 510(k) | K063346 | PRO OSTEON 500R | MQV | 2007-04-18 | View |
| 510(k) | K062494 | EBI OPTILOCK UPPER EXTREMITY PLATING SYSTEM | HRS | 2006-10-19 | View |
| 510(k) | K062810 | SOLITAIRE ANTERIOR SPINAL SYSTEM | MQP | 2006-10-17 | View |
| 510(k) | K062685 | EBI ARAY SPINAL SYSTEM | NKB | 2006-10-06 | View |
| 510(k) | K061978 | EBI, L.P.'S LINE EXTENSION TO THE ARRAY SPINAL SYSTEM | MNI | 2006-08-11 | View |
| 510(k) | K061441 | EBI 5.5 HELICAL FLANGE SPINAL SYSTEM | MNH | 2006-07-25 | View |
| 510(k) | K061563 | EBI ARRAY SPINAL SYSTEM | NKB | 2006-06-23 | View |
| 510(k) | K061016 | EBI ESL PEEK-OPTIMA SPINE SYSTEM | MQP | 2006-06-08 | View |
| 510(k) | K061098 | EBI OPTILOCK PERIARTICULAR PLATING SYSTEM | HRS | 2006-05-24 | View |
No matching devices.
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