Medical Device Manufacturer · US , Austin , TX

Ldr Spine USA - FDA 510(k) Cleared Devices

25 submissions · 25 cleared · Since 2005
25
Total
25
Cleared
0
Denied

Ldr Spine USA has 25 FDA 510(k) cleared orthopedic devices. Based in Austin, US.

Historical record: 25 cleared submissions from 2005 to 2016.

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
25 devices
1-12 of 25
Cleared Mar 31, 2016
Avenue L Lateral Lumbar Cage, Avenue T TLIF Cage System, ROI-A ALIF Cage...
K153495 · MAX
Orthopedic · 115d
Cleared Jan 25, 2016
FacetBRIDGE System
K152137 · MRW
Orthopedic · 178d
Cleared Dec 07, 2015
ROI-C Titanium-Coated Implant System
K151934 · OVE
Orthopedic · 146d
Cleared Sep 17, 2015
LDR Spine ROI-C Cervical Cage System
K150765 · OVE
Orthopedic · 177d
Cleared Sep 30, 2011
LDR SPINE ROI-A INTERBODY FUSION SYSTEM
K110327 · OVD
Orthopedic · 239d
Cleared Oct 15, 2010
LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
K102331 · MNI
Orthopedic · 59d
Cleared Sep 29, 2010
LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
K102265 · KWQ
Orthopedic · 50d
Cleared Mar 31, 2010
LDR SPINE USA SPINE TUNE TL SPINE SYSTEM
K100575 · MNI
Orthopedic · 30d
Cleared Jul 14, 2009
LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
K091088 · ODP
Orthopedic · 90d
Cleared Jun 25, 2009
MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM
K090507 · MAX
Orthopedic · 120d
Cleared Feb 12, 2009
LDR SPINE ROI-C IMPLANT
K083857 · MQP
Orthopedic · 50d
Cleared Feb 02, 2009
LDR SPINE ROI INTERBODY FUSION SYSTEM
K082262 · MAX
Orthopedic · 178d
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