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
-
1 to 6 of 6 Results
ProductCode: GDW Applicant: INTUITIVE SURGICAL, INC. Decision Date To: 06/04/2023
Results per Page
New Search  
Export all 6 Records to ExcelExport to Excel | Download Files | More About 510(k)
Device Name
Sort by Device Name [A-Z]
Sort by Device Name [Z-A]
Applicant
Sort by Applicant [A-Z]
Sort by Applicant [Z-A]
510(K)
Number
Sort by 510(k) Number [0-9]
Sort by 510(k) Number [9-0]
Decision
Date
Sort by Decision Date [0-9]
Sort by Decision Date [9-0]
8 mm sureform 30 curved-tip stapler, 8 mm sureform 30 stapler, sureform 30 reloads Intuitive Surgical, Inc. K211997 12/10/2021
sureform 45 curved tip, sureform 45 gray reload Intuitive Surgical, Inc. K190999 07/12/2019
endowrist stapler 45 system and stapler 45 reloads Intuitive Surgical, Inc. K171388 05/31/2017
endowrist stapler 45 instrument, endowrist stapler 45 reloads, endowrist stapler 30 instrument, endowrist stapler 30 reloads Intuitive Surgical, Inc. K170508 03/10/2017
is4000 stapler 30 instrument and stapler 30 reloads INTUITIVE SURGICAL, INC. K152421 03/04/2016
endowrist stapler 45 and stapler 45 reloads INTUITIVE SURGICAL, INC. K140553 07/25/2014
-
-