The purpose of this study is to leverage standard of care data on clinical outcomes following surgical procedures as indicated for each device.
* Performance Objective: To collect clinical outcomes and Patient Reported Outcome Measures (PROMs) data (as applicable) on subjects that have undergone surgical breast procedures utilizing one or more Stryker devices.
* Safety Objective: To collect data on safety events on the use of Stryker devices and/or related procedures
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject was ≥ 18 years of age at the time of the surgery
Patients who have undergone breast surgical procedures using MOLLI, SPY-PHI, and/or SPY AGENT GREEN
You may not be if
Subjects who are less than 1-month post-intervention
Concurrent participation in an interventional investigational clinical study at the time of initial surgery
Subjects whose surgery date was prior to January 2022.
Pregnant or lactating females at the time of initial surgery
Clareo Health | PROspect Registry :Post Market Clinical Follow-up Study
