The following data is part of a premarket notification filed by Black Box Medical with the FDA for Fuse Pedicle Screw System.
Device ID | K182283 |
510k Number | K182283 |
Device Name: | FUSE Pedicle Screw System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Black Box Medical 4516 East County Road 45 Midland, TX 79705 |
Contact | Todd Stanaford |
Correspondent | Daniel Lanois SurgOp Support 7512 Lancaster Gate Frisco, TX 75035 |
Product Code | NKB |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-08-23 |
Decision Date | 2018-10-23 |
Summary: | summary |