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 |