• 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 K171632
Device Name da Vinci Xi Surgical System
Applicant
Intuitive Surgical, Inc
1266 Kifer Road
Sunnyvale,  CA  94086
Applicant Contact Brandon Hansen
Correspondent
Domecus Consulting Services LLC
1171 Barroilhet Drive
Hillsborough,  CA  94010
Correspondent Contact Cindy Domecus
Regulation Number876.1500
Classification Product Code
NAY  
Date Received06/02/2017
Decision Date 09/19/2017
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
-
-