The following data is part of a premarket notification filed by Spineology Inc. with the FDA for Spineolgy Peek Bullet Lumber Interbody Fusion Device.
| Device ID | K111880 |
| 510k Number | K111880 |
| Device Name: | SPINEOLGY PEEK BULLET LUMBER INTERBODY FUSION DEVICE |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Spineology Inc. 7800 THIRD STREET N. SUITE 600 Saint Paul, MN 55128 |
| Contact | Bryan Becker |
| Correspondent | Bryan Becker Spineology Inc. 7800 THIRD STREET N. SUITE 600 Saint Paul, MN 55128 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-07-01 |
| Decision Date | 2011-09-26 |
| Summary: | summary |