FDA 510(k)

Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating

Número K: K260636 · 2026-06-18

RequerenteStryker Sustainability Solutions

Data da decisão2026-06-18

Código do produtoGEI

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K260636. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?

Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K260636.

When did Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating receive FDA 510(k) clearance?

Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating received FDA 510(k) clearance on 2026-06-18, under 510(k) number K260636.

Who is the listed applicant for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?

The FDA 510(k) record lists Stryker Sustainability Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?

The FDA product code for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is GEI.

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Fonte oficial

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