3F X 60 CM SINGLE LUMEN SILISONE VASCU-PICC, 4F X 60CM SINGLE LUMEN SILICONE VASCU-PICC, 5F X 60 CM SINGLE LUMEN SILICON

FDA 510(k)

FDA Class 2 ·General Hospital

SUTURE LOCK NAIL BONE ANCHOR WITH WHITE (KFX-W-200) & BLUE (KFX-B-200) FIBERFORCE SUTURE

FDA 510(k)

FDA Class 2 ·Orthopedic

AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

5.5 MM SUTURE LOCK BONE SCREW ANCHOR

FDA 510(k)

FDA Class 2 ·Orthopedic

KFX TISSUE FIXATION SYSTEM AND ACCESSORIES

FDA 510(k)

FDA Class 2 ·Orthopedic

FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

KFX PEEK BONE ANCHOR WITH PRE-ATTACHED SUTURES AND INSERTER HANDLE

FDA 510(k)

FDA Class 2 ·Orthopedic

KFX KNOTLESS FIXATION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

KFX APPIANFX PEEK FEMORAL IMPLANT WITH INSERTER

FDA 510(k)

FDA Class 2 ·Orthopedic

APPIANFX SUTURE ANCHOR (6MM) (5MM) APPIANFX TISSUE ANCHOR

FDA 510(k)

FDA Class 2 ·Orthopedic

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·Senza HFX iQ System, Senza HFX iQ IPG, HFX Trial Stimulator, HFX iQ Remote, HFX iQ Patient Application

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·HFX App

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval

FDA Class 3 ·INTEGRITY AFX DR (MODEL 5342) & SR (MODEL 5142) PULSE GENERATORS

Stimulator, Electrical, Implanted, For Parkinsonian Tremor

FDA Pre-Market Approval

FDA Class 3 ·Percept Deep Brain Stimulation Therapy System

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval

FDA Class 3 ·INTEGRITY AFX DR/INTEGRITY SR

Programmer, Pacemaker

FDA Pre-Market Approval

FDA Class 3 ·INTEGRITY/BRADYCARDIA REFERENCE/PATIENT MANUAL

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·Senza HFX iQ System

Programmer, Pacemaker

FDA Pre-Market Approval

FDA Class 3 ·INTEGRITY AFX DR MODEL 5346

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval

FDA Class 3 ·INTEGRITY AFX DR MODEL 5346

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·Senza HFX iQ System (model IPG3000)