Accel Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Accel Spine - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Accel Spine has 10 FDA 510(k) cleared orthopedic devices. Based in Dallas, US.
Historical record: 10 cleared submissions from 2012 to 2014.
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 - Accel Spine
10 devices
Cleared
Apr 14, 2014
PICASSO II MIS SPINAL SYSTEM
Orthopedic
75d
Cleared
Oct 09, 2013
CEZANNE II INTERBODY FUSION SYSTEM
Orthopedic
103d
Cleared
Sep 03, 2013
SPINAL INTERVERTEBRAL BODY FIXATION ORTHOSIS
Orthopedic
35d
Cleared
Aug 20, 2013
SPONDYLOLISTHESIS SPINAL FIXATION, SPINAL PEDICLE FIXATION
Orthopedic
21d
Cleared
Sep 26, 2012
ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
Orthopedic
120d
Cleared
Sep 21, 2012
DALI SPINAL FIXATION SYSTEM
Orthopedic
115d
Cleared
Sep 13, 2012
VAN GOGH ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
157d
Cleared
Aug 09, 2012
PICASSO MIS SPINAL FIXATION SYSTEM
Orthopedic
154d
Cleared
Aug 09, 2012
RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
Orthopedic
118d
Cleared
Jul 27, 2012
MATISSE ANTERIOR CERVICAL INTERBODY FUSION CAGE SYSTEM
Orthopedic
59d