The following data is part of a premarket notification filed by Alliance Partners, Llc. with the FDA for Alamo T.
| Device ID | K140303 |
| 510k Number | K140303 |
| Device Name: | ALAMO T |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | ALLIANCE PARTNERS, LLC. 4600 E SHELBY DR Memphis, TN 38118 |
| Contact | Kellen Hills |
| Correspondent | Kellen Hills ALLIANCE PARTNERS, LLC. 4600 E SHELBY DR Memphis, TN 38118 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-02-06 |
| Decision Date | 2014-04-21 |
| Summary: | summary |