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 |