SEARCH RESULTS FOR: Origin(1670 results)

MICROWIRE DEPTHALON ELECTRODE, 4 MICROWIRE CONTACTS, INLINE CONNECTOR

MICROWIRE DEPTHALON ELECTRODE, 16 MICROWIRE CONTACTS, MINI CONNECTOR

MICROWIRE DEPTHALON ELECTRODE, 8 MICROWIRE CONTACTS, INLINE CONNECTOR

MICROWIRE DEPTHALON ELECTRODE, 8 MICROWIRE CONTACTS, INLINE CONNECTOR

MICROWIRE DEPTHALON ELECTRODE, 16 MICROWIRE CONTACTS, 2 SHIELDED INLINE TAILS WITH 10CM LEAD

MICROWIRE DEPTHALON ELECTRODE, 16 MICROWIRE CONTACTS, 2 SHIELDED INLINE TAILS WITH 10CM LEAD

MICROWIRE DEPTHALON ELECTRODE, 16 MICROWIRE CONTACTS, 2 SHIELDED INLINE TAILS

MICROWIRE DEPTHALON ELECTRODE, 32 MICROWIRE CONTACTS, 3 SHIELDED INLINE TAILS

MICROWIRE DEPTHALON ELECTRODE, 32 MICROWIRE CONTACTS, 3 SHIELDED INLINE TAILS

MICROWIRE DEPTHALON ELECTRODE, 8 MICROWIRE CONTACTS, MINI CONNECTOR

PLATINUM ELECTRODE, WITH NEEDLE AND CABLE, NON-CRIMPED, 2 LOOSE CONNECTORS

PLATINUM ELECTRODE, WITH NEEDLE, WITHOUT CABLE, NON-CRIMPED, BLUE DEPTH STOP ON NEEDLE

PLATINUM ELECTRODE, WITH NEEDLE, WITHOUT CABLE, NON-CRIMPED

PLATINUM ELECTRODE, WITH NEEDLE, WITHOUT CABLE, CRIMPED

STAINLESS STEEL ELECTRODE, WITH NEEDLE, WITHOUT CABLE, NON-CRIMPED

STAINLESS STEEL ELECTRODE, WITH NEEDLE, WITHOUT CABLE, CRIMPED

SPHENOIDAL ELECTRODE EEG CABLE 1.5MM SOCKET SET

No Description

No Description

No Description

Instrument to use with ORIGIN implants

Instrument to use with ORIGIN implants

Instrument to use with ORIGIN implants

Instrument to use with ORIGIN implants

Instrument to use with ORIGIN implants

Omnia Medical VBR, Graft Packing Block

The Neurolutions System is a Brain-Computer-Interface (BCI) device developed for rehabilitation of upper extremity disability for chronic stroke patients. The device consists of the Neurolutions robotic handpiece, a biometric headset, and a Windows-based tablet computer. The Neurolutions System provides upper extremity rehabilitation using three separate modes: the main mode of therapy is referred to as the BCI or ‘thought’ mode, in which the patient’s hand is opened or closed by the Orthosis based on brain-signals received from the biometric headset; the second mode is referred to as a ‘volitional’ mode in which a patient actively opens and closes their hand with the System enabling independent range of motion; the third is a continuous passive motion (CPM) mode in which the System simply moves the patient’s hand passively through a comfortable range of motion in a repetitive fashion.

The Neurolutions System is a Brain-Computer-Interface (BCI) device developed for rehabilitation of upper extremity disability for chronic stroke patients. The device consists of the Neurolutions robotic handpiece, a biometric headset, and a Windows-based tablet computer. The Neurolutions System provides upper extremity rehabilitation using three separate modes: the main mode of therapy is referred to as the BCI or ‘thought’ mode, in which the patient’s hand is opened or closed by the Orthosis based on brain-signals received from the biometric headset; the second mode is referred to as a ‘volitional’ mode in which a patient actively opens and closes their hand with the System enabling independent range of motion; the third is a continuous passive motion (CPM) mode in which the System simply moves the patient’s hand passively through a comfortable range of motion in a repetitive fashion.

Rod, MIS, Lordotic 5.5X130mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion.

Rod, MIS, Lordotic 5.5X120mm. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion.