K261309
- 510(k) number
- K261309
- Device name
- Palisades Buttress Plate System
- Applicant
- Bethesda Medical Devices, LLC OH · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2026-07-16
- Date received
- 2026-04-21
- 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: K261309.pdf
Official FDA record: K261309
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.