Biedermann Motech GmbH
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) | K894184 | BIEDERMANN MOTECH UNIVERSAL SPINAL SYSTEM | JDN | 1990-04-25 | View |
| 510(k) | K900138 | MOTECH TITANIUM SURGICAL MESH | EZX | 1990-03-20 | View |
No matching devices.
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