Trephine

FDA classification

FDA Class 1 ·Trephine

Instrument, Cast Application/Removal, Manual

FDA classification

FDA Class 1 ·Instrument, Cast Application/Removal, Manual

Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented

Tube, Cement Ventilation

FDA classification

FDA Class 1 ·Tube, Cement Ventilation

Extractor

FDA classification

FDA Class 1 ·Extractor

Ankle Arthroplasty Implantation System

FDA classification

FDA Class 2 ·Ankle Arthroplasty Implantation System

Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uhmwpe, Pegged, Cemented, Polymer/Metal/Polymer

Crimper, Pin

FDA classification

FDA Class 1 ·Crimper, Pin

Rod, Fixation, Intramedullary And Accessories

FDA classification

FDA Class 2 ·Rod, Fixation, Intramedullary And Accessories

Set, Hollow Mill

FDA classification

FDA Class 1 ·Set, Hollow Mill

Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive

FDA classification

FDA Class 2 ·Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer, + Additive

Pin, Fixation, Smooth

FDA classification

FDA Class 2 ·Pin, Fixation, Smooth

Rod, Fixation, Intramedullary And Accessories, In-Vivo Cured, Light-Activated

FDA classification

FDA Class 2 ·Rod, Fixation, Intramedullary And Accessories, In-Vivo Cured, Light-Activated

Component, Traction, Invasive

FDA classification

FDA Class 2 ·Component, Traction, Invasive

Wire, Surgical

FDA classification

FDA Class 2 ·Wire, Surgical

Anterior Staple As Supplemental Fixation For Fusion

FDA classification

FDA Class 2 ·Anterior Staple As Supplemental Fixation For Fusion

Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices

FDA classification

FDA Class 2 ·Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices

Goniometer, Nonpowered

FDA classification

FDA Class 1 ·Goniometer, Nonpowered

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical

Prosthesis, Shoulder, Constrained, Metal/Metal Or Metal/Polymer Cemented

FDA classification

FDA Class 3 ·Prosthesis, Shoulder, Constrained, Metal/Metal Or Metal/Polymer Cemented