510(k) Report

Devices descending from K093533

404 later devices reach Zimmer Patient Specific Instruments System, Version 2.0 through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+9K253674Blueprint Patient-Specific InstrumentationStryker Corporation (Tornier, S.A.S.)20260—
+9K250108OptiVu™ ShoulderMr Surgical Solutions, LLC20251—
+9K250827aprevo® anterior lumbar interbody fusion device; aprevo® lateral lumbar interbody fusion…Carlsmed, Inc.20252—
+10K252170OptiVu™ ShoulderMr Surgical Solutions, LLC20250—