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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K121760

CAPSTONE SPINAL SYSTEM · Medtronic Sofamor Danek USA, Inc. · decided 2012-08-29 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
CAPSTONE® Spinal SystemX0105157MEDTRONIC SOFAMOR DANEK, INC.MAX00885074417615
CAPSTONE® Spinal SystemX0905247MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150912
CAPSTONE® Spinal SystemX1204271MEDTRONIC SOFAMOR DANEK, INC.MAX00885074372693
CAPSTONE® Spinal SystemX0905243MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150875
CAPSTONE® Spinal SystemX1204273MEDTRONIC SOFAMOR DANEK, INC.MAX00885074372730
CAPSTONE® Spinal SystemX0905248MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150929
CAPSTONE® Spinal SystemX1204274MEDTRONIC SOFAMOR DANEK, INC.MAX00885074372778
CAPSTONE® Spinal SystemX1204272MEDTRONIC SOFAMOR DANEK, INC.MAX00885074372723
CAPSTONE® Spinal SystemX0905244MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150882
CAPSTONE® Spinal SystemX0905252MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150967
CAPSTONE® Spinal SystemX0905251MEDTRONIC SOFAMOR DANEK, INC.MAX00613994150950