Ostex Intl., Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K011052 | OSTEOMARK NTX POINT OF CARE PRESCRIPTION HOME USE | JMM | 2001-07-30 | View |
| 510(k) | K983457 | OSTEOMARK NTX SERUM EIA | JMM | 1999-02-02 | View |
| 510(k) | K980518 | OSTEOMARK | JMM | 1998-03-06 | View |
| 510(k) | K961562 | OSTEOMARK | JMM | 1996-07-11 | View |
| 510(k) | K945946 | OSTEOMARK(R) | JMM | 1995-05-08 | View |
No matching devices.
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