K241259
- 510(k) number
- K241259
- Device name
- Amplatz Goose Neck Snare Kit
- Applicant
- Medtronic, Inc. MN · US
- Product code
- MMX — Device, Percutaneous Retrieval
- Decision date
- 2024-06-03
- Date received
- 2024-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K241259.pdf
Official FDA record: K241259
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.