NCT01914653View on ClinicalTrials.gov

SERI® Surgical Scaffold Postmarket Study of Soft Tissue Support and Repair in Breast Reconstruction

NACompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

June 30, 2013

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
Breast Reconstruction
Interventions
DEVICE

Silk surgical mesh

A CE Marked, 510(k) cleared, knitted, multi-filament, bioengineered, silk mesh indicated for use as a transitory scaffold for soft tissue support and repair

Trial Locations (1)

Unknown

Assuta Medical Center, Tel Aviv

All Listed Sponsors
lead

Sofregen Medical, Inc.

INDUSTRY

NCT01914653 - SERI® Surgical Scaffold Postmarket Study of Soft Tissue Support and Repair in Breast Reconstruction | Biotech Hunter | Biotech Hunter