K260636
- 510(k) number
- K260636
- Device name
- Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating
- Applicant
- Stryker Sustainability Solutions AZ · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-06-18
- Date received
- 2026-02-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K260636.pdf
Official FDA record: K260636
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.