Intervertebral Fusion Device With Integrated Fixation, Lumbar
FDA product code OVD · 179 cleared devices
Class 2
Orthopedic
- Regulation
- 21 CFR 888.3080
- Review panel
- OR
- Implant
- Yes
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2007-09-18 – 2026-09-11
Intended to stabilize lumbar spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental fixation.
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2016-02-18
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2016-01-13
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2013-09-18
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2013-09-13
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2013-08-28
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2013-05-17
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2013-04-25
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OVD
2013-04-16
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OVD
2013-03-18
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2013-03-05
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2012-11-01
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2012-10-25
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2012-10-11
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2012-07-26
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2012-07-26
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2012-06-27
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2012-03-27
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OVD
2012-03-19
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OVD
2012-03-16
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OVD
2012-03-13
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OVD
2011-10-04
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OVD
2011-09-30
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OVD
2011-09-09
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OVD
2011-08-04
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2011-05-20
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OVD
2011-04-04
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OVD
2011-03-30
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OVD
2011-02-10
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OVD
2011-01-12
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OVD
2010-12-03
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OVD
2010-09-30
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2010-09-02
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OVD
2010-07-20
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2010-06-16
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2010-03-24
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2010-03-09
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OVD
2010-03-05
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OVD
2009-12-15
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OVD
2009-11-17
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OVD
2009-02-13
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OVD
2008-12-22
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2008-11-05
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2008-09-11
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2008-08-28
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2008-07-02
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2008-07-02
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OVD
2008-06-25
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2008-06-04
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2007-10-12
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OVD
2007-09-18
INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC
View details →No matching devices.
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