Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K933867
›
Descendants
Devices descending from K933867
2 later devices reach Universal Inset Patella through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K971652
P.F.C. Sigma Inset Patella
Johnson & Johnson Professionals, Inc.
1997
1
—
+2
K241000
ATTUNE™ Revision Knee System; DePuy Knee Prosthesis System Universal Stem Extensions and…
Depuy Ireland UC
2024
0
—