K230724
- 510(k) number
- K230724
- Device name
- arcad® 2.0 Duo & Quadro osteosynthesis compressive staples
- Applicant
- Novastep FR
- Product code
- JDR — Staple, Fixation, Bone
- Decision date
- 2023-12-04
- Date received
- 2023-03-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K230724.pdf
Official FDA record: K230724
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.