K251436
- 510(k) number
- K251436
- Device name
- Resolve Anterior Cervical Plate System
- Applicant
- Pioneer Surgical Technology, Inc. MI · US
- Product code
- KWQ — Appliance, Fixation, Spinal Intervertebral Body
- Decision date
- 2025-07-11
- Date received
- 2025-05-08
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K251436.pdf
Official FDA record: K251436
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.