Rsb Spine, LLC
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K092540 | C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACER | ODP | 2010-01-27 | View |
| 510(k) | K092070 | INTERPLATE C | KWQ | 2009-10-06 | View |
| 510(k) | K081194 | INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD) | OVE | 2008-05-29 | View |
| 510(k) | K071922 | INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC | OVD | 2007-09-18 | View |
| 510(k) | K071372 | MODIFICATION TO: INTERPLATE VBR SYSTEM | MQP | 2007-06-11 | View |
| 510(k) | K070316 | INTERPLATE VBR SYSTEM | MQP | 2007-04-19 | View |
| 510(k) | K061401 | INTERPLATE VBR SYSTEM | MQP | 2006-08-18 | View |
No matching devices.
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