K240084
- 510(k) number
- K240084
- Device name
- V-STRUT® Vertebral Implant
- Applicant
- Hyprevention FR
- Product code
- NDN — Cement, Bone, Vertebroplasty
- Decision date
- 2024-02-09
- Date received
- 2024-01-11
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K240084.pdf
Official FDA record: K240084
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.