The Fixation Study

SeaSpine

Status: Active, not recruiting

Conditions: Degenerative Conditions, Neurologic

Treatments: Device: SeaSpine Non-Cervical Pedicle Screw Systems

Study type: Observational

Funder types: Industry

Identifiers

NCT04300777

SS-PMCF-1905

Details and patient eligibility

About

To perform a clinical evaluation of safety and performance for the SeaSpine Non- Cervical Pedicle Screw Systems

Full description

A multi-center, post-market, clinical evaluation for subjects implanted with the SeaSpine Non-Cervical Pedicle Screw Systems

Enrollment: 50 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Have undergone surgery
• Have undergone at least 12-months of postoperative follow-up

Exclusion criteria

• Any condition that the Investigator determines is unacceptable

Trial design

50 participants in 1 patient group

Treated with Non-Cervical Pedicle Screw Systems

Description:

50 patients who have been implanted with SeaSpine Non-Cervical Pedicle Screw Systems

Treatment:

Device: SeaSpine Non-Cervical Pedicle Screw Systems