PROspect Registry :Post Market Clinical Follow-up Study

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

Inclusion criteria

• 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

Exclusion criteria

• 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