
Specific Indication
For patients who fail conservative treatment, but who are not
candidates for a complete laminectomy or an irreversible
procedure such as fusion, functional interlaminar implants are the
answer.
Main indication: Radiographically confirmed moderate
to severe stenosis with neural element compromise resulting
in claudication and/or radicular symptoms isolated
to 1 or 2 levels, in the region of L1 to L5 with or without
concomitant low back pain including conditions such as stable grade
1 spondylolisthesis. Interlaminar stabilization is performed after
microsurgical decompression of stenosis at the affected level(s).
The coflex™ implant may also be used in up to 2 lumbar motion
segments adjacent to fused level(s).
Research Activities
Research activities include:
Instability (rotational or vertical) associated with recurrent
herniations
Large voluminous primary disc herniations
Adjunctive therapy for stabilizing levels above or below a fusion
("topping off") in the same procedure to minimize adjacent level
degeneration.
Conjunctive therapies to be envisioned:
Combination with nucleus replacements
Combination with total disc replacements with mild to
moderate facet degeneration.
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Press
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29.03.2010
PARADIGM SPINE
COMPLETES ENROLLMENT
IN PIVOTAL CLINICAL
STUDY OF COFLEX®
INTERLAMINAR TECHNOLOGY
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