510(k) Report

Devices descending from K232265

3 later devices reach BLUEPRINT™ Patient Specific Instrumentation through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K241491Blueprint Patient-Specific Instrumentation; Shoulder iD Primary Reversed GlenoidStryker Corporation (Tornier, S.A.S.)20241—
+1K241097Arthrex Virtual Implant Positioning (VIP) System SoftwareArthrex, Inc.20240—
+2K253674Blueprint Patient-Specific InstrumentationStryker Corporation (Tornier, S.A.S.)20260—