The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.
Study Type
OBSERVATIONAL
Enrollment
100,000
Unnamed facility
Birmingham, Alabama, United States
RECRUITINGUnnamed facility
Huntsville, Alabama, United States
RECRUITINGUnnamed facility
Chandler, Arizona, United States
RECRUITINGUnnamed facility
Phoenix, Arizona, United States
Safety and Effectiveness of Market Released products
Time frame: Every 6-12 months (Therapy-dependent)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Little Rock, Arkansas, United States
RECRUITINGUnnamed facility
Aliso Viejo, California, United States
RECRUITINGUnnamed facility
Chula Vista, California, United States
RECRUITINGUnnamed facility
Colton, California, United States
RECRUITINGUnnamed facility
La Jolla, California, United States
RECRUITINGUnnamed facility
Los Angeles, California, United States
RECRUITING...and 378 more locations