Mindways Software, Inc.
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) | K030330 | CTXA HIP EXTENDED REFERENCE DATA | KGI | 2003-06-20 | View |
| 510(k) | K002113 | CTXA HIP; CTXA; QCT PRO CTXA HIP | KGI | 2001-12-04 | View |
No matching devices.
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