
Nobles Medical Technologies Ii, Inc.
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SRM-STITCH 8F SRM-STITCH 8F WITH GUIDEWIRE is an FDA 510(k)-cleared medical device (K113763) manufactured by Nobles Medical Technologies Ii, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 2012. Regulation: 8.