The following data is part of a premarket notification filed by Accel Spine with the FDA for Renoir Posterior Cervial Fixation System.
| Device ID | K121136 |
| 510k Number | K121136 |
| Device Name: | RENOIR POSTERIOR CERVIAL FIXATION SYSTEM |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| 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 | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-13 |
| Decision Date | 2012-08-09 |
| Summary: | summary |