The following data is part of a premarket notification filed by Globus Medical, Inc. with the FDA for Revolve Additional Implants.
Device ID | K111449 |
510k Number | K111449 |
Device Name: | REVOLVE ADDITIONAL IMPLANTS |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 |
Contact | Sarah Marie Fitzgerald |
Correspondent | Sarah Marie Fitzgerald GLOBUS MEDICAL, INC. 2560 GENERAL ARMISTEAD AVE. VALLEY FORGE BUSINESS CENTER Audubon, PA 19403 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-05-25 |
Decision Date | 2011-08-17 |
Summary: | summary |