The following data is part of a premarket notification filed by Ngmedical Gmbh with the FDA for Bee Ha Cage.
| Device ID | K203444 |
| 510k Number | K203444 |
| Device Name: | BEE HA Cage |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | NGMedical GmbH Talsperrenblick 5 Nonnweiler, DE 66620 |
| Contact | Stella Hahn |
| Correspondent | Christine Scifert MRC Global, LLC 9085 E. Mineral Cir., Suite 110 Centennial, CO 80112 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-11-23 |
| Decision Date | 2021-03-18 |