K241034
- 510(k) number
- K241034
- Device name
- Meta+ Bone Cement & M.U.S.T. Fenestrated Pedicle Screw System
- Applicant
- Medacta International S.A. CH
- Product code
- PML — Bone Cement, Posterior Screw Augmentation
- Decision date
- 2024-06-12
- Date received
- 2024-04-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K241034.pdf
Official FDA record: K241034
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.