Medical Device Manufacturer · US , Dallas , TX

Accel Spine - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2012
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
1-10 of 10
Cleared Apr 14, 2014
PICASSO II MIS SPINAL SYSTEM
K140219 · NKB
Orthopedic · 75d
Cleared Oct 09, 2013
CEZANNE II INTERBODY FUSION SYSTEM
K131981 · MAX
Orthopedic · 103d
Cleared Sep 03, 2013
SPINAL INTERVERTEBRAL BODY FIXATION ORTHOSIS
K132366 · KWQ
Orthopedic · 35d
Cleared Aug 20, 2013
SPONDYLOLISTHESIS SPINAL FIXATION, SPINAL PEDICLE FIXATION
K132365 · MNI
Orthopedic · 21d
Cleared Sep 26, 2012
ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM
K121567 · MAX
Orthopedic · 120d
Cleared Sep 21, 2012
DALI SPINAL FIXATION SYSTEM
K121568 · NKB
Orthopedic · 115d
Cleared Sep 13, 2012
VAN GOGH ANTERIOR CERVICAL PLATE SYSTEM
K121078 · KWQ
Orthopedic · 157d
Cleared Aug 09, 2012
PICASSO MIS SPINAL FIXATION SYSTEM
K120714 · NKB
Orthopedic · 154d
Cleared Aug 09, 2012
RENOIR POSTERIOR CERVIAL FIXATION SYSTEM
K121136 · KWP
Orthopedic · 118d
Cleared Jul 27, 2012
MATISSE ANTERIOR CERVICAL INTERBODY FUSION CAGE SYSTEM
K121569 · ODP
Orthopedic · 59d
Filters
Filter by Specialty
All10 Orthopedic 10