K233741
- 510(k) number
- K233741
- Device name
- Hoffmann LRF System
- Applicant
- Stryker GmbH CH
- Product code
- KTT — Appliance, Fixation, Nail/Blade/Plate Combination, M
- Decision date
- 2023-12-21
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K233741.pdf
Official FDA record: K233741
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.