DESIGNED WITH PURPOSE

The S-LIFT (Sagittal Lumbar Interbody Fusion Technology) is a Less Exposure Surgery technology whose whole system is cohesively designed to minimize incisions and tissue disruption while maximizing volume for bone fusion.

DESIGNED WITH PURPOSE

The S-LIFT (Sagittal Lumbar Interbody Fusion Technology) is a Less Exposure Surgery technology whose whole system is cohesively designed to minimize incisions and tissue disruption while maximizing volume for bone fusion.

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HOW S-LIFT INNOVATES

S-LIFT’s design allows for a lateral approach to the anatomy, which enables a smaller incision size. Its architecture provides rigidity, increased strength and graft volume.

Open-Back Design
Open-Back Design

A proprietary open back design allows for graft placement after insertion to maximize volume for bone fusion.

RIGID Construct
RIGID Construct

S-LIFT's thick walls create an incredibly rigid cage that restores disc height and minimizes fear of breakage during insertion or loading.

Aggressive Teeth
Aggressive Teeth

Several aggressive teeth span the entire interbody, creating purchase on both sides of the vertebral body to minimize chances of cage expulsion.

Split Rib Design
Split Rib Design

A unique split rib design increases rigidity and robustness of the cage while also allowing for more graft to fill the interbody space during post-packing. This innovative feature creates opportunity for a fusion mass to form throughout the cage.

All-PEEK Design
All-PEEK Design

S-LIFT's PEEK design provides support while maintaining radiolucency. Combined with strategically placed tantalum markers, surgeons are given maximum visibility of not just device placement, but also recovery results.

Lordotic & Straight Cages
Lordotic & Straight Cages

A range of lordotic and straight cages accommodates differing levels of patient lordosis.

'LESR-TRI' Lateral Retractor
"LESR-TRI" Lateral Retractor

S-LIFT's lateral access retractor allows for positional stability and a lateral approach that creates a safe technique for a large interbody. This versatile retractor accommodates virtually any technique and anatomy.

4th Blade Configuration
4th Blade Configuration

A fourth blade option on S-LIFT’s three blade retractor provides an anterior blade to create a larger window and to prevent anterior tissue creep.

S-LIFT ADOPTION DATA

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days on the market

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surgeon users

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interbodies sold & used

MAKING S-LIFT

Vito Lore, Director of Innovation,
on Developing S-LIFT

CASE STUDIES & RESEARCH

S-LIFT WORKS WITH

LESR-Tri
VIEW PRODUCT
MISquito
VIEW PRODUCT
INDICATIONS
The SpineFrontier Lumbar Interbody Fusion Device System (Dorado IBC, Dorado PLIFT, Dorado ELIFT, Dorado ALIFT, Dorado TILT, Dorado TLIFT, Dorado Wide, and Ursa S-LIFT) is intended for intervertebral body fusion of the spine of skeletally mature patients, using autogenous bone graft to facilitate fusion. The device is indicated for use in patients with degenerative disc disease (DDD) at one or two contiguous spinal levels from L2-S1. These DDD patients may also have up to Grade I spondylolisthesis or retrolisthesis at the involved level(s).

The LESR-Tri Retractor is intended to manipulate tissue or for use with other devices in orthopedic surgery. This instrument may be used during surgical procedures requiring lateral access to the lumbar spine for use by, or as directed by a surgeon.

The SpineFrontier® PedFuse® Pedicle Screw System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute instabilities or deformities of the thoracic, lumbar, and sacral: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion (Pseudarthrosis). In addition, the SpineFrontier® PedFuse® Pedicle Screw System is indicated for the treatment of severe spondylolisthesis (Grade 3 and 4) of the L5-S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine. When used in a percutaneous approach with MIS instrumentation, the SpineFrontier® PedFuse® Pedicle Screw System is intended to provide immobilization and stabilization of spine segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, failed previous fusion (Pseudarthrosis) and severe spondylolisthesis (Grade 3 and 4) of the L5-S1 vertebra in skeletally mature patients receiving fusion by autogenous bone graft, with the device fixed or attached to the lumbar and sacral spine.

Degenerative disc disease is defined as discogenic back pain with degeneration of the disc confirmed by history or radiographic studies. These patients should be skeletally mature and have had six months of non-operative treatment.The SpineFrontier Lumbar Intervertebral Body Fusion Device System is intended to be used with supplemental spinal fixation system(s) cleared for use in the lumbar spine.