K253888
- 510(k) number
- K253888
- Device name
- MOLLI 2 System
- Applicant
- Stryker Endoscopy CA · US
- Product code
- NEU — Marker, Radiographic, Implantable
- Decision date
- 2025-12-31
- Date received
- 2025-12-04
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.4 MB · U.S. public domain
Also available from FDA: K253888.pdf
Official FDA record: K253888
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.