Activortho, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2019-07-26
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K191817 | ActivOrtho Continuous Compression Screw System | HWC | 2019-07-26 | View |
| 510(k) | K181610 | ActivOrtho Nitinol Compression Screw System | HWC | 2019-03-12 | View |
No matching devices.