K241018
- 510(k) number
- K241018
- Device name
- KLS Martin Orthopedic Implants - MR Conditional
- Applicant
- KLS-Martin L.P. FL · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-07-12
- Date received
- 2024-04-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K241018.pdf
Official FDA record: K241018
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.