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 5 of 5 Results
ProductCode: FTM Applicant: SYNOVIS SURGICAL INNOVATIONS Decision Date To: 03/29/2023
Results per Page
New Search  
Export all 5 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]
veritas collagen matrix (dry) SYNOVIS SURGICAL INNOVATIONS K083039 11/26/2008
veritas collagen matrix SYNOVIS SURGICAL INNOVATIONS K062915 12/06/2006
peri-strips staple line reinforcement-sleeve configuration, peri-strips staple line reinforcement-strip configuration SYNOVIS SURGICAL INNOVATIONS K040119 03/17/2004
veritas dry collagen matrix, veritas dry or veritas psd SYNOVIS SURGICAL INNOVATIONS K041669 10/27/2004
veritas collagen matrix SYNOVIS SURGICAL INNOVATIONS K030879 04/24/2003
-
-