Ionics Medical Corp.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K081673 | DYN-ALIF ANTEROLATERAL INTERVERTEBRAL BODY FUSION DEVICE | MAX | 2008-11-14 | View |
| 510(k) | K983667 | IONICS LEVANTE INTERVERTEBRAL PILLAR, EXPANDABLE | MQP | 2000-07-05 | View |
No matching devices.
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