K241695
- 510(k) number
- K241695
- Device name
- Extremity All Suture System
- Applicant
- Field Orthopaedics AU
- Product code
- MBI — Fastener, Fixation, Nondegradable, Soft Tissue
- Decision date
- 2024-09-12
- Date received
- 2024-06-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241695.pdf
Official FDA record: K241695
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.