Lanx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lanx, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Lanx, Inc. has 23 FDA 510(k) cleared orthopedic devices. Based in Broomfield, US.
Historical record: 23 cleared submissions from 2009 to 2013.
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 - Lanx, Inc.
23 devices
Cleared
Jul 12, 2013
LANX FUSION SYSTEM
Orthopedic
44d
Cleared
May 24, 2013
LANX SPINAL FIXATION SYSTEM
Orthopedic
30d
Cleared
Mar 18, 2013
LANX FUSION SYSTEM- SA
Orthopedic
101d
Cleared
Sep 10, 2012
LANX SPINAL FIZATION SYSTEM
Orthopedic
131d
Cleared
Aug 17, 2012
LANX SPINAL FIXATION SYSTEM
Orthopedic
29d
Cleared
Aug 02, 2012
LANX SPINAL FIXATION SYSTEM
Orthopedic
31d
Cleared
Dec 19, 2011
LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
Orthopedic
28d
Cleared
Dec 16, 2011
LANX CERVICAL SA
Orthopedic
120d
Cleared
Apr 15, 2011
LANX SPINAL FIXATION SYSTEM
Orthopedic
178d
Cleared
Mar 25, 2011
LANX SPINAL SYSTEM
Orthopedic
143d
Cleared
Mar 23, 2011
LANX LATERAL
Orthopedic
98d
Cleared
Feb 28, 2011
LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
Orthopedic
75d