Ldr Spine USA
FDA 510(k) medical device clearances.
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.