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FDA 510(k)

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

K-Number: K230251 · 2023-03-28

ApplicantStryker Sustainability Solutions
Decision Date2023-03-28
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 2023-03-28 under approval number K230251. 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 2023-03-28. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K230251.

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 2023-03-28, under approval number K230251.

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.

Other Devices by Stryker Sustainability Solutions

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Related Devices (Code: NUJ)

K161086Reprocessed Harmonic Shears with Adaptive Tissue Technology (36 cm), Reprocessed Harmonic Shears with Adaptive Tissue Technology (23cm)Sterilmed, Inc. K160333Medline ReNewal Reprocessed LigaSure Blunt Tip Open Sealer/DividerSurgical Instrument Service and Savings, Inc. K153745Medline ReNewal Reprocessed LigaSure Impact Open Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren K152134Reprocessed Vessel SealerSterilmed, Inc. K152313Medline ReNewal Reprocessed Endopath Endoscopic InstrumentsSurgical Instrument Services and Savings, Inc. K172608Medline ReNewal Reprocessed Stryker SERF AS Energy ProbesSurgical Instrument Service and Savings, Inc.

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.

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