510(k) Report

Devices descending from K983365

12 later devices reach Aesculap Minop System through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K182211Aurora Surgiscope SystemRebound Therapeutics Corporation20194—
+1K132931Apollo SystemPenumbra, Inc.20145—
+1K014149Paediscope, Model # P010A and PF011AAesculap, Inc.20020—
+2K191861Aurora Surgiscope SystemRebound Therapeutics20193—
+2K171332Artemis Neuro Evacuation DevicePenumbra, Inc.20172—
+2K152699Apollo SystemPenumbra, Inc.20164—
+3K201308Axonpen, Axonmonitor, Axonbox, TabletClearmind Biomedical20201—
+3K201840Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box)Rebound Therapeutics202021
+3K181731MR Compatible Aspiration KitMri Interventions, Inc.20180—
+4K250752AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)Integra LifeSciences Corporation20250—
+4K232618Aurora Surgiscope SystemRebound Therapeutics Corporation202301
+4K230125Neuroblade SystemClearmind Biomedical20230—