Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name System, Surgical, Computer Controlled Instrument
510(k) Number K140553
Device Name ENDOWRIST STAPLER 45 AND STAPLER 45 RELOADS
Applicant
INTUITIVE SURGICAL, INC.
1266 KIFER RD
SUNNYVALE,  CA  94086
Applicant Contact DAWN CHANG
Correspondent
INTUITIVE SURGICAL, INC.
1266 KIFER RD
SUNNYVALE,  CA  94086
Correspondent Contact DAWN CHANG
Regulation Number876.1500
Classification Product Code
NAY  
Subsequent Product Code
GDW  
Date Received03/04/2014
Decision Date 07/25/2014
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
-
-