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 |