The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Protex Stabilization System.
| Device ID | K040442 | 
| 510k Number | K040442 | 
| Device Name: | PROTEX STABILIZATION SYSTEM | 
| Classification | Orthosis, Spondylolisthesis Spinal Fixation | 
| Applicant | GLOBUS MEDICAL, INC. 303 SCHELL LANE Phoenixville, PA 19460 | 
| Contact | Kelly J Baker | 
| Correspondent | Kelly J Baker GLOBUS MEDICAL, INC. 303 SCHELL LANE Phoenixville, PA 19460  | 
| Product Code | MNH | 
| Subsequent Product Code | KWI | 
| Subsequent Product Code | KWQ | 
| Subsequent Product Code | MNI | 
| Subsequent Product Code | NKB | 
| CFR Regulation Number | 888.3070 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2004-02-20 | 
| Decision Date | 2004-05-20 | 
| Summary: | summary |