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 |