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FDA 510(k) Applications Submitted by Benjamin V. Keller
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180056
01/08/2018
Genesys Spine AIS-C Cervical Anchored Interbody System
Genesys Spine
K181295
05/16/2018
Genesys Spine AIS-C Cervical Stand-Alone System
Genesys Spine
K191489
06/04/2019
Genesys Spine 3DP Cervical Interbody System
Genesys Spine
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