The following data is part of a premarket notification filed by Aegis Spine with the FDA for Zespin Si Joint Fusion System, Megacerfix Posterior Cervical Fixation System, Megacerfix Anterior Cervical Plate System, Spinema Lumbar Plate System.
| Device ID | K210035 |
| 510k Number | K210035 |
| Device Name: | ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System |
| Classification | Sacroiliac Joint Fixation |
| Applicant | Aegis Spine 9781 S. Meridian Blvd, Ste 300 Englewood, CO 80112 |
| Contact | Kay Kwon |
| Correspondent | Meredith Lee May Empirical Testing Corp. 4628 Northpark Drive Colorado Springs, CO 80918 |
| Product Code | OUR |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | NKG |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-01-06 |
| Decision Date | 2021-02-16 |
| Summary: | summary |