The following data is part of a premarket notification filed by Accel Spine with the FDA for Picasso Mis Spinal Fixation System.
Device ID | K120714 |
510k Number | K120714 |
Device Name: | PICASSO MIS SPINAL FIXATION SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
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 | NKB |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-03-08 |
Decision Date | 2012-08-09 |
Summary: | summary |