The following data is part of a premarket notification filed by Pantheon Spinal with the FDA for Pantheon Spinal Ibfd System.
| Device ID | K113781 |
| 510k Number | K113781 |
| Device Name: | PANTHEON SPINAL IBFD SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | PANTHEON SPINAL 9442 CAPITAL OF TEXAS HWY NORTH - SUITE 900 Austin, TX 78759 |
| Contact | Scott Spann |
| Correspondent | Scott Spann PANTHEON SPINAL 9442 CAPITAL OF TEXAS HWY NORTH - SUITE 900 Austin, TX 78759 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-12-22 |
| Decision Date | 2013-04-26 |