K252737
- 510(k) number
- K252737
- Device name
- DeGen Medical Latitude-C AM Cervical Interbody Fusion System
- Applicant
- Degen Medical SC · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2025-10-10
- Date received
- 2025-08-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K252737.pdf
Official FDA record: K252737
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.