Ldr Spine USA, Inc. is one of 18445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ldr Spine USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VerteFIT Corpectomy Cage System, Avenue® T TLIF Cage, FacetBRIDGE® System
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
Cleared
May 16, 2017
VerteFIT Corpectomy Cage System
Orthopedic
288d
Cleared
Sep 28, 2016
Avenue® T TLIF Cage
Orthopedic
155d
Cleared
Aug 04, 2016
FacetBRIDGE® System
Orthopedic
35d
Cleared
Jun 11, 2015
Avenue T TLIF Cage
Orthopedic
267d
Cleared
Mar 07, 2014
INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
Orthopedic
126d
Cleared
Feb 01, 2013
EASYSPINE SYSTEM
Orthopedic
119d
Cleared
Aug 24, 2012
LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE,...
Orthopedic
135d
Cleared
Jul 26, 2012
LDR SPINE USA AVENUE L INTERBODY FUSION
Orthopedic
262d
Cleared
Jun 27, 2012
LDR SPINE SPINETUNE TL SPINAL SYSTEM
Orthopedic
106d
Cleared
Dec 29, 2011
LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS
Orthopedic
28d