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 |