The following data is part of a premarket notification filed by Globus Medical Inc. with the FDA for Hedron Lumbar Spacers.
Device ID | K191391 |
510k Number | K191391 |
Device Name: | HEDRON Lumbar Spacers |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 |
Contact | Kelly Baker |
Correspondent | Kelly Baker Globus Medical Inc. 2560 General Armistead Ave. Audubon, PA 19403 |
Product Code | MAX |
Subsequent Product Code | OVD |
Subsequent Product Code | PHM |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-05-24 |
Decision Date | 2019-09-18 |
Summary: | summary |