Reliance Medical Systems
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) | K181118 | Reliance Lumbar IBF System | OVD | 2019-01-09 | View |
| 510(k) | K180687 | Reliance Lumber IBF System | MAX | 2018-05-15 | View |
| 510(k) | K101112 | RELIANCE SPINAL SCREW SYSTEM | KWP | 2010-11-04 | View |
No matching devices.
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