Pinnacle Spine Group, LLC
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K172349 | InFill® Interbody Fusion Device | MAX | 2017-12-14 | View |
| 510(k) | K124012 | INFILL OBLIQUE TLIF DEVICE | MAX | 2013-06-04 | View |
| 510(k) | K121476 | INFILL GRAFT DELIVERY SYSTEM | FMF | 2012-08-29 | View |
| 510(k) | K121733 | INFILL INTERVERTEBRAL BODY FUSION DEVICE | MAX | 2012-07-13 | View |
| 510(k) | K111632 | INFILL GRAFT DELIVERY SYSTEM | FMF | 2011-08-11 | View |
| 510(k) | K103729 | INFILL INTERVERTEBRAL BODY FUSION DEVICE | MAX | 2011-04-18 | View |
No matching devices.
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