Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K041894
›
Descendants
Devices descending from K041894
4 later devices reach Orthofiber through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K094028
CP-Fiber (Orthofiber)
Cp Medical
2010
0
—
+1
K082518
Dual Needle Suture Passer System
Cayenne Medical, Inc.
2009
0
—
+1
K071796
Capsew Plication System
Cayenne Medical, Inc.
2007
0
—
+1
K050150
Mani Needle & Suture Pack
Mani, Inc.
2005
0
—