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 10 of 20 Results
ProductCode: FTL Applicant: ETHICON, INC. Decision Date To: 11/27/2021
 
 1 
 2 
 > 
Results per Page
New Search  
Export all 20 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]
vicryl ETHICON, INC. K810428 03/13/1981
prolene polypropylene mesh nonabsorbable synthetic surgical mesh ETHICON, INC. K962530 08/09/1996
prolene polypropylene mesh hernia device nonabsorbable synthetic surgical mesh ETHICON, INC. K972412 09/10/1997
modification of prolene (polypropylene) hernia system, nonabsorbable synthetic surgical mesh ETHICON, INC. K984220 02/23/1999
prolene soft (polypropylene), nonabsorbabale synthetic surgical mesh ETHICON, INC. K001122 05/23/2000
vypro mesh, vicryl prolene partially absorbable synthetic surgical mesh ETHICON, INC. K002672 11/22/2000
prolene (polypropylene) 3d patch, nonabsorbable synthetic surgical mesh ETHICON, INC. K010722 04/27/2001
proceed trilaminate surgical mesh ETHICON, INC. K031925 09/17/2003
ultrapro mesh ETHICON, INC. K033337 04/01/2004
vicryl * mesh bag ETHICON, INC. K051701 09/29/2005
-
-