K232897
- 510(k) number
- K232897
- Device name
- Arthrex Small External Fixation System
- Applicant
- Arthrex, Inc. FL · US
- Product code
- KTT — Appliance, Fixation, Nail/Blade/Plate Combination, M
- Decision date
- 2023-10-18
- Date received
- 2023-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232897.pdf
Official FDA record: K232897
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.