The following data is part of a premarket notification filed by Spinal Balance Inc. with the FDA for Libra Pedicle Screw System.
Device ID | K151770 |
510k Number | K151770 |
Device Name: | Libra Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Spinal Balance Inc. 1510 North Westwood Avenue Toledo, OH 43606 |
Contact | Anand Agarwal |
Correspondent | Karen E. Warden BackRoads Consulting Inc. P.O. Box 566 Chesterland, OH 44026 |
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 | 2015-06-30 |
Decision Date | 2015-11-20 |
Summary: | summary |