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An FDA advisory panel voted 6-1 that Stryker’s PMA for its OP-1 Putty for uninstrumented posterolateral fusion for the treatment of lumbar spondylolisthesis was not approvable. Stryker was seeking this approval based on 24 months of clinical outcome data and 36 month CT scan and reoperation rates
Read MoreIndividuals suffering from a common back condition known as spinal stenosis improve more with surgery than with non-surgical treatment, according to a study.
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