510(k) Report

Devices descending from K063172

12 later devices reach Arthrocare Cavity Spinewand through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K091310Ablation Instrument, Model 1635; Ablation Multiplex Catheter, Model 1682Dfine, Inc.201011—
+2K142480OsteoCool V-2 RF Ablation SystemBaylis Medical Company, Inc.20159—
+2K111523Osteocool (TM) RF Ablation SystemBaylis Medical Co., Inc.20120—
+3K152057OsteoCool V-3 RF Ablation SystemBaylis Medical Company, Inc.20158—
+4K161949OsteoCool V-3 RF Ablation SystemBaylis Medical Company, Inc.20177—
+5K192406AveCure BT Microwave Ablation SystemMedwaves, Inc.20200—
+5K182497OsteoCool RF Ablation SystemMedtronic Sofamor Danek USA, Inc.20195—
+6K233830OsteoCool™ 2.0 RF Ablation SystemMedtronic Sofamor Danek USA, Inc.20241—
+6K223303Spinery™ RF Ablation SystemAxon Spine Medical System20230—
+6K221074OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion DeviceStryker Corporation20222—
+7K253656OsteoCool™ RF Ablation System; OsteoCool™ 2.0 RF Ablation SystemMedtronic Sofamor Danek USA, Inc.20260—
+7K250327OptaBlate Radiofrequency (RF) Generator SystemStryker Instruments20250—