The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Intercontinental Plate-spacer.
| Device ID | K103382 | 
| 510k Number | K103382 | 
| Device Name: | INTERCONTINENTAL PLATE-SPACER | 
| Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar | 
| Applicant | GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403 | 
| Contact | Kelly J Baker | 
| Correspondent | Kelly J Baker GLOBUS MEDICAL INC. 2560 GENERAL ARMISTEAD AVE. Audubon, PA 19403  | 
| Product Code | OVD | 
| CFR Regulation Number | 888.3080 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2010-11-18 | 
| Decision Date | 2011-05-20 | 
| Summary: | summary |