Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
SeaSpine, Inc.
To gain observational, prospective, real-world clinical, and radiographic data in order to evaluate continued safety and performance following the implantation of SeaSpine products.
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Have been treated with at least one SeaSpine product.
Have obtained radiographic imaging, as part of the standard of care, at the following time points: preoperative and postoperative.
Have obtained at least one preoperative patient-reported outcome measure, as part of the standard of care.
Patient is planned, per standard of care, to be assessed with radiographic imaging and consistent patient-reported outcome measure(s) from preoperative through at least two scheduled follow-up visits.
You may not be if
Was not implanted with at least one SeaSpine product during operation
Any other condition that the Investigator determines is unacceptable for enrollment into this registry
