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FDA 510(k) Applications Submitted by CLAUDIA HILL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170512
02/21/2017
Altus Spine Titanium Interbody Fusion System
Altus Partners, LLC
K160976
04/07/2016
Altus Spine Interbody Fusion System
ALTUS PARTNERS, LLC
K171329
05/05/2017
Altus Spine Titanium Interbody Fusion System
Altus Partners, LLC
K151648
06/18/2015
Altus Spine Pedicle Screw System, Altus Spine MIS Pedicle Screw System, Valencia Pedicle Screw System, Valencia MIS Pedicle Screw System
Altus Partners, LLC
K132280
07/23/2013
ALTUS SPINE PEDICLE SCREW SYSTEM
ALTUS PARTNERS
K163061
11/01/2016
Altus Spine Cervical Plate System
Altus Partners, LLC
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