NCT02016612 - Seri Surgical Scaffold Support of the Lower Pole of the Breast | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

November 30, 2015

Study Completion Date

November 30, 2016

Conditions

Recurrent Ptosis of the Breast

Interventions

DEVICE

Seri Surgical Scaffold

An FDA approved Bioabsorbable mesh Seri Surgical Scaffold will be utilized in the study as an internal hammock mesh support of the breast.

Trial Locations (2)

Bengtson Center for Aesthetics and Plastic Surgery, Grand Rapids

Center for Aesthetics and Plastic Surgery, Grand Rapids