FDA 510(k) Applications Submitted by ALEXANDRA BECK

FDA 510(k) Number Submission Date Device Name Applicant
K151064 04/20/2015 Solitaire-C Cervical Spacer System, C-Thru Anterior Spinal System, Breckenridge Small Intervertebral Body Fusion System BIOMET SPINE
K151974 07/16/2015 Polaris Spinal System BIOMET SPINE
K152622 09/14/2015 Alta ACDF System BIOMET SPINE


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