K240530
- 510(k) number
- K240530
- Device name
- DynaNail Mini Tapered Hybrid
- Applicant
- MedShape, Inc. GA · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2024-03-21
- Date received
- 2024-02-23
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K240530.pdf
Official FDA record: K240530
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.