Centinel Spine, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173347 | STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX | MAX | 2018-05-08 | View |
| 510(k) | K130461 | STALIF X | OVD | 2013-08-28 | View |
| 510(k) | K120819 | STALIF C | OVE | 2012-08-31 | View |
No matching devices.
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