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 |