K260340
- 510(k) number
- K260340
- Device name
- HC BIOLOGICS OSTEOPOINT PEEK CAGES, HC BIOLOGICS OSTEOPOINT CERVICAL PEEK CAGES, HC BIOLOGICS OSTEOPOINT LUMBAR PEEK CAGES
- Applicant
- HC Biologics, LLC FL · US
- Product code
- ODP — Intervertebral Fusion Device With Bone Graft, Cervic
- Decision date
- 2026-04-13
- Date received
- 2026-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K260340.pdf
Official FDA record: K260340
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.