The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Spinefrontier Lumbar Ibf System.
| Device ID | K111553 |
| 510k Number | K111553 |
| Device Name: | SPINEFRONTIER LUMBAR IBF SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
| Contact | Hannah Crowe |
| Correspondent | Hannah Crowe SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-06-03 |
| Decision Date | 2011-09-28 |
| Summary: | summary |