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510(k) Data Aggregation
K Number
K241258Device Name
Ingenix Spinal System
Manufacturer
Date Cleared
2024-06-04
(29 days)
Product Code
Regulation Number
888.3070Why did this record match?
Applicant Name (Manufacturer) :
Ingenium Spine
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Ingenix™ Spinal System is intended to provide immobilization of spinal segments in sketally mature patients as an adjunct to fusion in the treatment of the following acute and chromic instabilities of thoracic, lumbar, and sacral spine; degenerative spondylolisthesis, with objective evidence of neurological impairment, fracture, dislocation, scoliosis, spinal tumor, severe spondylolisthesis (Grade 3 and 4) of the L5-S1 vertebra with autogenous bone graft, and failed previous fusion (pseudarthrosis).
Device Description
The Ingenix™ Spinal System (originally cleared as "Arisstos Spinal System") is an internal fixation device for spinal surgery consisting of rods, screws, and connectors available in various sizes to accommodate patient anatomy. A series of manual instruments intended to assist in the insertion and placement of the implants, such as taps, drivers, and rod benders, is provided in separate instrument trays.
The subject rods, screws, and connectors are manufactured of Ti-6Al-4V titanium alloy per ASTM F136. Additionally, 5.5mm and 6.0mm cobalt chrome rods are also available, conforming to ASTM F1537. All instruments are manufactured from stainless steel, aluminum, and select polymers.
The subject submission seeks to gain clearance for the following:
- . Minor modifications made to screws
- . Size expansion for the polyaxial deformity screws
- . Sterile packaging of a kit configuration
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K Number
K173126Device Name
Arisstos Spinal System
Manufacturer
Date Cleared
2017-12-05
(67 days)
Regulation Number
888.3070Why did this record match?
Applicant Name (Manufacturer) :
Ingenium Spine
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
Intended Use
The Arisstos™ Spinal System is intended to provide immobilization of spinal segments in skeletally mature patients as an adjunct to fusion in the following acute and chronic instabilities or deformities of the thoracic, lumbar and sacral spine: degenerative spondylolisthesis, with objective evidence of neurological impairment, fracture, dislocation, scoliosis, spinal tumor and failed previous fusion (pseudarthrosis).
The Arisstos™ Spinal System is indicated for the treatment of severe spondylolisthesis (Grade 3 and 4) of the LS-S1 vertebra in skeletally mature patients undergoing fusion by autogenous bone grafting having implants attached to the lumbar and sacral spine with removal of implants after the attainment of a solid fusion.
Device Description
The Arisstos™ Spinal System is an internal fixation device for spinal surgery consisting of rods, screws, hooks and connectors available in various lengths, diameters, and configurations to enable close conformance to patient anatomy. A series of manual instruments intended to assist in the insertion and placement of the implants is provided in separate trays.
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