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 |