Core Essence Orthopaedics, LLC

Core Essence Orthopaedics, LLC — FDA 510(k) Submissions

Core Essence Orthopaedics, LLC has submitted 3 FDA 510(k) premarket notifications since 2007, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Staple, Fixation, Bone, Fastener, Fixation, Nondegradable, Soft Tissue, Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile . Use the specialty filter in the sidebar to narrow results.