Shoulder Innovations, Inc.

Shoulder Innovations, Inc. — FDA 510(k) Submissions

Shoulder Innovations, Inc. has submitted 7 FDA 510(k) premarket notifications since 2018, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Shoulder Prosthesis, Reverse Configuration, Prosthesis, Shoulder, Non-constrained, Metal/polymer Cemented, Prosthesis, Total Anatomic Shoulder, Uncemented Metaphyseal Humeral Stem With No Diaphyseal Incursion, Semi-constrained, Prosthesis, Shoulder, Semi-constrained, Metal/polymer, Uncemented . Use the specialty filter in the sidebar to narrow results.