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 |