Ldr Spine USA
Ldr Spine USA holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2016.
Top product codes for Ldr Spine USA
Recent clearances by Ldr Spine USA
- K153495 — Avenue L Lateral Lumbar Cage, Avenue T TLIF Cage System, ROI-A ALIF Cage System, ROI-T Implant System
- K152137 — FacetBRIDGE System
- K151934 — ROI-C Titanium-Coated Implant System
- K150765 — LDR Spine ROI-C Cervical Cage System
- K110327 — LDR SPINE ROI-A INTERBODY FUSION SYSTEM
- K102331 — LDR SPINE USA SPINETUNE TL SPINAL SYSTEM
- K102265 — LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
- K100575 — LDR SPINE USA SPINE TUNE TL SPINE SYSTEM
- K091088 — LDR SPINE CERVICAL INTERBODY FUSION SYSTEM
- K090507 — MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM
- K083857 — LDR SPINE ROI-C IMPLANT
- K082262 — LDR SPINE ROI INTERBODY FUSION SYSTEM
- K082592 — LDR SPINE EASYSPINE SYSTEM
- K080728 — LDR SPINE ROI-C IMPLANT
- K080569 — LDR SPINE ROI-T IMPLANT
- K080572 — LDR SPINE ROI-A IMPLANT
- K072132 — LDR SPINE ROI-T SYSTEM
- K070341 — LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM
- K063794 — MODIFICATION TO EASYSPINE SYSTEM
- K061462 — BF+ (PH)
- K061017 — EASYSPINE SYSTEM
- K043479 — MC+ PARTIAL VBR
- K043349 — OPEN RADIOTRANSPARENT INTERSOMATIC IMPLANT (ROI)
- K043094 — EASYSPINE SYSTEM
- K043347 — BF+
Data sourced from openFDA. This site is unofficial and independent of the FDA.