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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact