The following data is part of a premarket notification filed by Carbofix Orthopedics Ltd. with the FDA for Carboclear® Pedicle Screw System.
| Device ID | K173487 |
| 510k Number | K173487 |
| Device Name: | CarboClear® Pedicle Screw System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | CarboFix Orthopedics Ltd. 11 Ha’hoshlim St. Herzeliya, IL 4672411 |
| Contact | Hila Wachsler-avrahami |
| Correspondent | Hila Wachsler-avrahami CarboFix Orthopedics Ltd. 11 Ha’hoshlim St. Herzeliya, IL 4672411 |
| Product Code | NKB |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-11-13 |
| Decision Date | 2018-07-18 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CARBOCLEAR 86654176 5283412 Live/Registered |
CarboFix In Orthopedics LLC 2015-06-07 |