The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Sustain R Tps Spacers, Patriot Tps Spacers, Caliber Tps Spacer, Coalition Tps Spacers, Independence Tps Spacer, Fortify -r Tps Corpectomy Spacer, Fortify I-r Tps Corpectomy Spacer, Xpand -r Tps Corpectomy Spacer, Niko Tps Corpectomy Spacer.
Device ID | K143578 |
510k Number | K143578 |
Device Name: | SUSTAIN R TPS Spacers, PATRIOT TPS Spacers, CALIBER TPS Spacer, COALITION TPS Spacers, INDEPENDENCE TPS Spacer, FORTIFY -R TPS Corpectomy Spacer, FORTIFY I-R TPS Corpectomy Spacer, XPand -R TPS Corpectomy Spacer, NIKO TPS Corpectomy Spacer |
Classification | Intervertebral Fusion Device With Bone Graft, 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 AVENUE Audubon, PA 19403 |
Product Code | MAX |
Subsequent Product Code | MQP |
Subsequent Product Code | ODP |
Subsequent Product Code | OVD |
Subsequent Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-12-17 |
Decision Date | 2016-04-13 |
Summary: | summary |