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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name staple, implantable
510(k) Number K140560
Device Name ECHELON FLEX POWERED PLUS ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60MM, STANDARD, ECHELON FLEX POWERED PLUS ARTICULATING
Applicant
ETHICON ENDO-SURGERY, LLC
4545 CREEK ROAD
cincinnati,  OH  45242
Applicant Contact asifa vonhof
Correspondent
ETHICON ENDO-SURGERY, LLC
4545 CREEK ROAD
cincinnati,  OH  45242
Correspondent Contact asifa vonhof
Regulation Number878.4750
Classification Product Code
GDW  
Date Received03/05/2014
Decision Date 04/22/2014
Decision substantially equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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