Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Reprocessed LigaSure Maryland Jaw Sealer/Divider

K-Number: K180499 · 2018-04-23

ApplicantStryker Sustainability Solutions
Decision Date2018-04-23
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Reprocessed LigaSure Maryland Jaw Sealer/Divider is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2018-04-23 under approval number K180499. 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 Maryland Jaw Sealer/Divider?

Reprocessed LigaSure Maryland Jaw Sealer/Divider is a medical device that received FDA 510(k) clearance on 2018-04-23. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K180499.

When was Reprocessed LigaSure Maryland Jaw Sealer/Divider approved by the FDA?

Reprocessed LigaSure Maryland Jaw Sealer/Divider received FDA 510(k) clearance on 2018-04-23, under approval number K180499.

What company makes Reprocessed LigaSure Maryland Jaw Sealer/Divider?

Reprocessed LigaSure Maryland Jaw Sealer/Divider is manufactured by Stryker Sustainability Solutions.

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 Devices by Stryker Sustainability Solutions

K153415Reprocessed Stryker External Fixation Devices K172856Reprocessed LigaSure Blunt Tip Laparoscopic Sealer/Divider K170456Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology K161693Reprocessed HARMONIC ACE+7, 5 mm Diameter Shears with Advanced Hemostasis K180451Reprocessed LigaSure Impact without Nano-coating Large Jaw, Open Sealer/Divider K182238Reprocessed ViewFlex Xtra ICE Catheter

View all 24 devices →

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.

↑