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# Orthopedic devices: recent FDA 510(k) clearances, page 2 of 2

Records 51 to 53 of the 53 newest listed for this hub. Source: U.S. FDA openFDA.

[1](/hub/fdapulse/specialty_type/orthopedic--510k-clearances) 2

| Record | Specialty | Type | Date |
|---|---|---|---|
| RIVA® Posterior Fixation System with NanoACTIV Surface Technology; RIVA® Anchor Sacroiliac Fixation System with NanoACTIV Surface Technology (K262193): 510(k) cleared for Xenix Medical | Orthopedic | 510(k) | 2026-09-14 |
| Innovasis AxTiHA® Stand-Alone ALIF System;Innovasis TxTiHA® IBF System;Innovasis HAtetracell®-C Titanium Cervical IBF System (K262025): 510(k) cleared for INNO Holdings Inc. DBA Innovasis | Orthopedic | 510(k) | 2026-09-11 |
| Mg OSTEOREVIVE™;Mg OSTEOCRETE™ (K262230): 510(k) cleared for Bone Solutions, Inc. | Orthopedic | 510(k) | 2026-09-11 |

[1](/hub/fdapulse/specialty_type/orthopedic--510k-clearances) 2

[All FDAPulse record reports](/hub/fdapulse/records)

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