510(k) Report

Devices descending from K122183

10 later devices reach Augment and Screw, Psa Type through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K210695CPM Medical Consultants Tibial Revision Knee SystemCpm Medical Consultants, LLC20210—
+1K190100USTAR II SystemUnited Orthopedic Corporation201925
+1K131864U2 Tibial Baseplate- Cma Type, Tibial Insert and AugmentUnited Orthopedic Corporation20145—
+2K252303Stem Extension Line (USTAR II System)United Orthopedic Corporation20250—
+2K243656U2 Total Knee System – PF+ Patella; USTAR II System– PF+ PatellaUnited Orthopedic Corporation20250—
+2K222700Tibial baseplate, Tibial insertUnited Orthopedic Corporation20220—
+2K161705U2 Total Knee System E-XPE productsUnited Orthopedic Corporation20171—
+2K152430All Poly Tibial ComponentUnited Orthopedic Corporation20160—
+2K150829U2 Total Knee System- Additional SizesUnited Orthopedic Corporation20153—
+3K210961U2 Total Knee System, XPE Tibial Insert, PS PLUSUnited Orthopedic Corporation20210—