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Ldr Spine USA, Inc.

10 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
VerteFIT Corpectomy Cage System (K162133)Ldr Spine USA, Inc.2017-05-16
Avenue® T TLIF Cage (K161173)Ldr Spine USA, Inc.2016-09-28
FacetBRIDGE® System (K161798)Ldr Spine USA, Inc.2016-08-04
Avenue T TLIF Cage (K142645)Ldr Spine USA, Inc.2015-06-11
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM (K133363)Ldr Spine USA, Inc.2014-03-07
EASYSPINE SYSTEM (K123134)Ldr Spine USA, Inc.2013-02-01
LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S (K121103)Ldr Spine USA, Inc.2012-08-24
LDR SPINE USA AVENUE L INTERBODY FUSION (K113285)Ldr Spine USA, Inc.2012-07-26
LDR SPINE SPINETUNE TL SPINAL SYSTEM (K120760)Ldr Spine USA, Inc.2012-06-27
LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS (K113559)Ldr Spine USA, Inc.2011-12-29

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Every clearance here is in the API, with alerts when new ones post.