LinkBio Corp.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2025-02-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K241470 | CORE Shoulder System | QHE | 2025-02-20 | View |
| 510(k) | K190181 | Instruments for LINK MEGASYSTEM-C Family | KRO | 2019-10-25 | View |
No matching devices.