510(k) K230251

Device
Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
Applicant
Stryker Sustainability Solutions
510(k) number
K230251
Product code
NUJ
Decision
Substantially Equivalent (SESE)
Decision date
2023-03-28
Date received
2023-01-30
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Scott English
Address
1810 W Dr.Ake Dr. Tempe AZ US 85283 85283

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code NUJ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K172608Medline ReNewal Reprocessed Stryker SERF AS Energy ProbesSurgical Instrument Service and Savings, Inc.2017-10-18
K171324Medline ReNewal Reprocessed ArthroCare ArthroWands and Smith & Nephew DyonicsSurgical Instrument Service and Savings, Inc.2017-06-23
K162751Medline ReNewal Reprocessed Ligasure Curved, Small Jaw Open Sealer/DividerSurgical Instrument Services and Savings, Inc.2017-05-01
K161086Reprocessed Harmonic Shears with Adaptive Tissue Technology (36 cm), Reprocessed Harmonic Shears with Adaptive Tissue Technology (23cm)Sterilmed, Inc.2016-09-20