SurGenTec LLC
The goal of this observational, ambispective study is to collect real world patient outcomes to characterize the safety and effectiveness of OsteoFlo HydroFiber when used to promote fusion in the lumbar spine.
Inclusion Criteria: * Skeletally mature and age ≥ 18 years of age at the time of surgery. * Previously implanted with OsteoFlo HydroFiber in one or two contiguous vertebral level(s) in the lumbar (L1-S1) spine. * OsteoFlo HydroFiber was mixed with saline, blood, or bone marrow aspirate prior to use in the index procedure. * Be 6-months (180 -10/+30 days) post-surgery at the time of informed consent and at the6-month visit. * Be willing and able to comply with the study protocol requirements. * For prospective visit cohort, be willing to sign the study-specific Informed Consent Form. Exclusio…
Observational study of subjects previously implanted with OsteoFlo HydroFiber.
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