Acme Spine, LLC
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) | K071824 | ACME TALON PEDICLE SCREW | MNI | 2007-09-04 | View |
| 510(k) | K001044 | ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM | MNH | 2000-11-03 | View |
No matching devices.
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