The following data is part of a premarket notification filed by Integra Spine (integra Lifesciences) with the FDA for Lateral Fusion Device.
Device ID | K112986 |
510k Number | K112986 |
Device Name: | LATERAL FUSION DEVICE |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | INTEGRA SPINE (INTEGRA LIFESCIENCES) 1153 MEDINA ROAD Medina, OH 44256 |
Contact | Dale Davison |
Correspondent | Dale Davison INTEGRA SPINE (INTEGRA LIFESCIENCES) 1153 MEDINA ROAD Medina, OH 44256 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-10-06 |
Decision Date | 2012-05-01 |
Summary: | summary |