The following data is part of a premarket notification filed by Accel Spine with the FDA for Spondylolisthesis Spinal Fixation, Spinal Pedicle Fixation.
| Device ID | K132365 |
| 510k Number | K132365 |
| Device Name: | SPONDYLOLISTHESIS SPINAL FIXATION, SPINAL PEDICLE FIXATION |
| Classification | Orthosis, Spinal Pedicle Fixation |
| Applicant | ACCEL SPINE 14901 QUORUM DR. STE. 125 Dallas, TX 75254 |
| Contact | Aekta Patel |
| Correspondent | Aekta Patel ACCEL SPINE 14901 QUORUM DR. STE. 125 Dallas, TX 75254 |
| Product Code | MNI |
| Subsequent Product Code | KWP |
| Subsequent Product Code | MNH |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-07-30 |
| Decision Date | 2013-08-20 |
| Summary: | summary |