K243742
- 510(k) number
- K243742
- Device name
- Arthrex DynaNite Nitinol Staples
- Applicant
- Arthrex, Inc. FL · US
- Product code
- JDR — Staple, Fixation, Bone
- Decision date
- 2025-01-31
- Date received
- 2024-12-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K243742.pdf
Official FDA record: K243742
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.