Ldr Spine Usa

FDA Filings

This page includes the latest FDA filings for Ldr Spine Usa. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Filings

Device Company	Device	Date
PMA P110002S022 LDR Spine USA	Mobi-C Cervical Disc Prosthesis (one-level indications)	2019-11-13
PMA P110002S020 LDR Spine USA	Mobi-C Cervical Disc Prosthesis	2018-05-30
PMA P110002S021 LDR Spine USA	LDR Spine Mobi-C Cervical Disc Prosthesis (One Level)	2018-05-15
PMA P110002S019 LDR Spine USA	MOBI-C Cervical Disc Prosthesis	2017-06-02
PMA P110002S018 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)	2017-05-23
PMA P110002S015 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)	2017-05-05
PMA P110002S016 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS.	2017-03-03
PMN K153495 LDR Spine USA	Avenue L Lateral Lumbar Cage, Avenue T TLIF Cage System, ROI-A ALIF Cage System, ROI-T Implant System	2016-03-31
PMA P110002S011 LDR Spine USA	THE MOBI-C CERVICAL DISC PROSTHESIS	2016-01-27
PMN K152137 LDR SPINE USA	FacetBRIDGE System	2016-01-25
PMA P110002S013 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2016-01-21
PMN K151934 LDR SPINE USA	ROI-C Titanium-Coated Implant System	2015-12-07
PMA P110002S010 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2015-10-06
PMN K150765 LDR SPINE USA	LDR Spine ROI-C Cervical Cage System	2015-09-17
PMA P110002S012 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2015-06-30
PMA P110002S009 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2015-02-05
PMA P110002S008 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)	2014-12-29
PMA P110002S007 LDR Spine USA	LDR SPINE MOBI-C CERVICAL DISC PROTHESIS (ONE LEVEL INDICATION)	2014-07-23
PMA P110002S005 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS (ONE LEVEL)	2014-07-15
PMA P110002S002 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2014-06-03
PMA P110002S001 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2014-05-27
PMA P110002S006 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2014-05-02
PMA P110002S004 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS FOR USE AT ONE OR TWO LEVELS	2014-02-21
PMA P110002S003 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS	2013-12-18
PMA P110002 LDR Spine USA	MOBI-C CERVICAL DISC PROSTHESIS (ONE-LEVEL INDICATION)	2013-08-07
PMN K110327 LDR SPINE USA	LDR SPINE ROI-A INTERBODY FUSION SYSTEM	2011-09-30
PMN K102331 LDR SPINE USA	LDR SPINE USA SPINETUNE TL SPINAL SYSTEM	2010-10-15
PMN K102265 LDR SPINE USA	LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM	2010-09-29
PMN K100575 LDR SPINE USA	LDR SPINE USA SPINE TUNE TL SPINE SYSTEM	2010-03-31
PMN K091088 LDR SPINE USA	LDR SPINE CERVICAL INTERBODY FUSION SYSTEM	2009-07-14
PMN K090507 LDR SPINE USA	MODIFICATION TO LDR SPINE ROI INTERBODY FUSION SYSTEM; ROI-A IMPLANT SYSTEM	2009-06-25
PMN K083857 LDR SPINE USA	LDR SPINE ROI-C IMPLANT	2009-02-12
PMN K082262 LDR SPINE USA	LDR SPINE ROI INTERBODY FUSION SYSTEM	2009-02-02
PMN K082592 LDR SPINE USA	LDR SPINE EASYSPINE SYSTEM	2008-10-08
PMN K080728 LDR SPINE USA	LDR SPINE ROI-C IMPLANT	2008-05-29
PMN K080569 LDR SPINE USA	LDR SPINE ROI-T IMPLANT	2008-05-07
PMN K080572 LDR SPINE USA	LDR SPINE ROI-A IMPLANT	2008-04-07
PMN K072132 LDR SPINE USA	LDR SPINE ROI-T SYSTEM	2007-08-30
PMN K070341 LDR SPINE USA	LDR SPINE EASYSPINE POSTERIOR OSTEOSYNTHESIS SYSTEM	2007-08-08
PMN K063794 LDR SPINE USA	MODIFICATION TO EASYSPINE SYSTEM	2007-01-24
PMN K061462 LDR SPINE USA	BF+ (PH)	2006-12-15
PMN K061017 LDR SPINE USA	EASYSPINE SYSTEM	2006-08-10
PMN K043479 LDR SPINE USA	MC+ PARTIAL VBR	2005-06-30
PMN K043349 LDR SPINE USA	OPEN RADIOTRANSPARENT INTERSOMATIC IMPLANT (ROI)	2005-06-29
PMN K043094 LDR SPINE USA	EASYSPINE SYSTEM	2005-02-11

Similar & Related FDA Registered Companies

• LDR SPINE USA, INC.