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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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