The following data is part of a premarket notification filed by Accel Spine with the FDA for Oracle Lumbar Intervertebral Body Fusion Cage System.
| Device ID | K121567 |
| 510k Number | K121567 |
| Device Name: | ORACLE LUMBAR INTERVERTEBRAL BODY FUSION CAGE SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | ACCEL SPINE 14850 Quorum Dr Ste 220 Dallas, TX 75254 |
| Contact | Daniel Chon |
| Correspondent | Daniel Chon ACCEL SPINE 14850 Quorum Dr Ste 220 Dallas, TX 75254 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-05-29 |
| Decision Date | 2012-09-26 |
| Summary: | summary |