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 |