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Clinique
By Spineart

JULIET®AN Study #14001

Symptomatic degenerative disc diseases treated by anterior lumbar arthrodesis with JULIET®AN and rhBMP2. A prospective safety and effectiveness study
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BAGUERA®C Study #16002

Cervical Arthroplasty using BAGUERA® C: A two-year, prospective, clinical follow-up data registry. Retrospective radiographic evaluation
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BAGUERA®C Study #16001

Cervical Arthroplasty using BAGUERA® C: A two-year, prospective, clinical follow-up data registry. Retrospective clinical analysis results
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JULIET®TL Study #30001

The JULIET®TL, lumbar intersomatic Poly-Ether-Ether-Ketone cage used for symptomatic degenerative disc diseases treatment by arthrodesis. Safety and effectiveness evaluation after two years follow-up
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TRYPTIK®CA Study #32001

Spinal degenerative discopathy treated by decompression and anterior arthrodesis with intersomatic Poly-Ether-Ether-Ketone anatomical cervical cage TRYPTIK®CA. Evaluation of safety and effectiveness
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TRYPTIK®MC Study #33001

Cervico-brachial neuralgia treated by decompression and anterior arthrodesis using intersomatic poly-ether-ether-ketone and titanium cervical anatomical modular cage-plate TRYPTIK®MC. Evaluation of safety and effectiveness.
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JULIET®OL Study #52001

The JULIET®OL, lumbar intersomatic poly-ether-ether-ketone cage used for symptomatic degenerative disc diseases treatment by arthrodesis. Safety and effectiveness evaluation after two years follow-up
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JULIET®PO study #12001

The JULIET®PO, lumbar intersomatic poly-ether-ether-ketone cage used for symptomatic degenerative disc diseases treatment by arthrodesis. Safety and effectiveness evaluation after two years follow-up
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JULIET® PO study #12002

The JULIET®PO, lumbar intersomatic Poly-Ether-Ether-Ketone cage used for symptomatic degenerative disc diseases treatment by arthrodesis. Safety and effectiveness evaluation after five years follow-up
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