Osteon, 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) | K891582 | MODIFIED OSTEOANALYZER (# SPSHA110/220) | KGI | 1989-09-12 | View |
| 510(k) | K843922 | OSTEON BONE MINERAL ANALYZER | KGI | 1985-04-02 | View |
No matching devices.
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