K241276
- 510(k) number
- K241276
- Device name
- Vector Pedicle Screw System
- Applicant
- Innovasis, Inc. UT · US
- Product code
- NKB — Thoracolumbosacral Pedicle Screw System
- Decision date
- 2024-05-20
- Date received
- 2024-05-06
- 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: K241276.pdf
Official FDA record: K241276
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.