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FDA 510(k)

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)

K-Number: K220411 · 2022-05-13

Decision Date2022-05-13
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2022-05-13 under approval number K220411. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is a medical device that received FDA 510(k) clearance on 2022-05-13. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K220411.

When was Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) approved by the FDA?

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) received FDA 510(k) clearance on 2022-05-13, under approval number K220411.

What company makes Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)?

The FDA product code for Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A) is NUJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.