K234051
- 510(k) number
- K234051
- Device name
- Minuteman G5 MIS Fusion Plate; Minuteman G1(Posterior Fusion Plate /HA Posterior Fusion Plate); HA Minuteman G3-R MIS Fusion Plate; Minuteman G3/HA Minuteman G3
- Applicant
- Spinal Simplicity, LLC KS · US
- Product code
- PEK — Spinous Process Plate
- Decision date
- 2024-01-18
- Date received
- 2023-12-21
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K234051.pdf
Official FDA record: K234051
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.