K243195
- 510(k) number
- K243195
- Device name
- Arthrex SS VAL and VAL KreuLock Compression Screw System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2025-01-10
- Date received
- 2024-10-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K243195.pdf
Official FDA record: K243195
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.