Orthogem Limited
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) | K110787 | TRIPORE TDD (HA), TRIPORE TDD (BP90), TRIPORE TDD (BP15) | MQV | 2011-04-21 | View |
| 510(k) | K070132 | TRIPORE, MODELS HA, BP90, BP15 | MQV | 2007-07-13 | View |
No matching devices.
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