The following data is part of a premarket notification filed by Eisertech, Llc with the FDA for Cervical Cage.
| Device ID | K110915 |
| 510k Number | K110915 |
| Device Name: | CERVICAL CAGE |
| Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
| Applicant | EISERTECH, LLC 2555 FRONT STREET San Diego, CA 92103 |
| Contact | Lukas Eisermann |
| Correspondent | Lukas Eisermann EISERTECH, LLC 2555 FRONT STREET San Diego, CA 92103 |
| Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-04-01 |
| Decision Date | 2011-07-22 |
| Summary: | summary |