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 |