Stereotaxis, Inc.
FDA 510(k) medical device clearances.
Top product codes for Stereotaxis, Inc.
Recent clearances by Stereotaxis, Inc.
- K253473 — Synchrony
- K251792 — Stereotaxis GenesisX RMN with Navigant Workstation (NWS)
- K250590 — MAGiC Sweep EP Mapping Catheter
- K193147 — Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive System
- K192775 — Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and Cardiodri
- K183027 — Steerable catheter control system
- K150312 — Vdrive system, Vdrive Duo, Vdrive with V-Sono
- K141530 — VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CAS
- K140804 — VDRIVE WITH V-LOOP/ VDRIVE DUO
- K133396 — VDRIVE WITH V-SONO
- K122659 — VDRIVE W/V-SONO
- K093092 — ODYSSEY WORKSTATION
- K080637 — POWERASSET RADIOFREQUENCY GUIDWIRE, MODEL VARIOUS
- K072371 — ODYSSEY WORKSTATION
- K071029 — CARDIODRIVE CATHETER ADVANCEMENT SYSTEM (CAS)
- K060967 — NIOBE MAGNETIC NAVIGATION SYSTEM W/NAVIGANT WORKSTATION
- K042850 — CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)
- K051760 — NAVIGANT WORKSTATION WITH NIOBE MAGNETIC NAVIGATION SYSTEM, MODEL NWS05
- K051373 — CRONUS GUIDEWIRE, MODEL 001-001470-1
- K051374 — CARDIODRIVE CATHETER ADVANCEMENT SYSTEM
- K043457 — MODIFICATION TO ENDOVASCULAR GUIDE WIRE
- K042854 — STEREOTAXIS ENDOVASCULAR GUIDE WIRE
- K032937 — NAVIGANT MAGNETIC NAVIGATION WORKSTATION 2.1 (NWS2) MODEL, 020-004500
- K021802 — STEREOTAXIS CATHETER ADVANCER SYSTEM
- K021555 — STEREOTAXIS NIOBE MAGNETIC NAVIGATION SYSTEM
- K021363 — ENDOVASCULAR GUIDE WIRE
- K022565 — TELSTAR BIPLANE DIGITAL IMAGING SYSTEM [TIS] MODEL 030-000915
- K013484 — TELSTAR MAGNETIC NAVIGATION SYSTEMS [MNS}, TELSTAR BI-PLANE DIGITAL IMAGING SYSTEM, NIOBE ELECTROPHYSIOLOGY MAPPING CATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.