K261271
- 510(k) number
- K261271
- Device name
- Cable-Ready® Cable Grip System
- Applicant
- Pioneer Surgical Technology, Inc. MI · US
- Product code
- JDQ — Cerclage, Fixation
- Decision date
- 2026-07-16
- Date received
- 2026-04-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K261271.pdf
Official FDA record: K261271
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.