FDA 510(k) Applications Submitted by LDR SPINE USA INC.

FDA 510(k) Number Submission Date Device Name Applicant
K121103 04/11/2012 LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S LDR SPINE USA INC.
K142645 09/17/2014 Avenue T TLIF Cage LDR SPINE USA INC.
K120760 03/13/2012 LDR SPINE SPINETUNE TL SPINAL SYSTEM LDR SPINE USA INC.
K113559 12/01/2011 LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS LDR SPINE USA INC.
K123134 10/05/2012 EASYSPINE SYSTEM LDR SPINE USA INC.
K113285 11/07/2011 LDR SPINE USA AVENUE L INTERBODY FUSION LDR SPINE USA INC.


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