Overview
A long-term (24 and 30 months) follow-up extension, prospective, non-interventional, open label study for data collection from subjects who underwent prior MIMS® inferonasal surgery, in continuation of the previous clinical investigation with the MIMS® Device (MMS-EEU-5).
Eligibility
Inclusion Criteria:
- Subject who underwent MIMS® inferonasal procedure, and surgery was performed not earlier than 24 months from enrollment