Medical Device Manufacturer · US , Austin , TX

Ldr Spine USA, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2011
10
Total
10
Cleared
0
Denied

Ldr Spine USA, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Austin, US.

Historical record: 10 cleared submissions from 2011 to 2017.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ldr Spine USA, Inc.
10 devices
1-10 of 10
Cleared May 16, 2017
VerteFIT Corpectomy Cage System
K162133 · MQP
Orthopedic · 288d
Cleared Sep 28, 2016
Avenue® T TLIF Cage
K161173 · OVD
Orthopedic · 155d
Cleared Aug 04, 2016
FacetBRIDGE® System
K161798 · MRW
Orthopedic · 35d
Cleared Jun 11, 2015
Avenue T TLIF Cage
K142645 · OVD
Orthopedic · 267d
Cleared Mar 07, 2014
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
K133363 · PEK
Orthopedic · 126d
Cleared Feb 01, 2013
EASYSPINE SYSTEM
K123134 · NKB
Orthopedic · 119d
Cleared Aug 24, 2012
LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE,...
K121103 · NKB
Orthopedic · 135d
Cleared Jul 26, 2012
LDR SPINE USA AVENUE L INTERBODY FUSION
K113285 · OVD
Orthopedic · 262d
Cleared Jun 27, 2012
LDR SPINE SPINETUNE TL SPINAL SYSTEM
K120760 · MNH
Orthopedic · 106d
Cleared Dec 29, 2011
LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS
K113559 · ODP
Orthopedic · 28d
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