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 |