The following data is part of a premarket notification filed by Innovative Surgical Designs, Inc. with the FDA for True Spinal Fixation System.
Device ID | K170710 |
510k Number | K170710 |
Device Name: | True Spinal Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Innovative Surgical Designs, Inc. 3903 S. Walnut St. Bloomington, IN 47401 |
Contact | Jon Rinehart |
Correspondent | Jon Rinehart Innovative Surgical Designs, Inc. 3903 South Walnut Street Bloomington, IN 47401 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-08 |
Decision Date | 2017-07-14 |