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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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