Reprocessed LigaSure Maryland Jaw Sealer/Divider
K-Number: K180499 · 2018-04-23
Device Summary
Frequently Asked Questions
What is the Reprocessed LigaSure Maryland Jaw Sealer/Divider?
Reprocessed LigaSure Maryland Jaw Sealer/Divider is a medical device that received FDA 510(k) clearance on 2018-04-23. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K180499.
When did Reprocessed LigaSure Maryland Jaw Sealer/Divider receive FDA 510(k) clearance?
Reprocessed LigaSure Maryland Jaw Sealer/Divider received FDA 510(k) clearance on 2018-04-23, under 510(k) number K180499.
Who is the listed applicant for Reprocessed LigaSure Maryland Jaw Sealer/Divider?
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 Reprocessed LigaSure Maryland Jaw Sealer/Divider?
The FDA product code for Reprocessed LigaSure Maryland Jaw Sealer/Divider is NUJ.
Other records listing Stryker Sustainability Solutions as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NUJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.