K241314
- 510(k) number
- K241314
- Device name
- KLS Martin Oral-Max Implants MR Conditional (bundled)
- Applicant
- KLS-Martin L.P. FL · US
- Product code
- JEY — Plate, Bone
- Decision date
- 2024-08-16
- Date received
- 2024-05-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K241314.pdf
Official FDA record: K241314
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.