The following data is part of a premarket notification filed by Aegis Spine, Inc. with the FDA for Zespin Si Joint Fusion System, Paeon Posterior Cervical Fixation System, Paeon Anterior Cervical Plate System, Spinema Lumbar Plate System.
| Device ID | K221050 |
| 510k Number | K221050 |
| Device Name: | ZESPIN SI Joint Fusion System, Paeon Posterior Cervical Fixation System, Paeon Anterior Cervical Plate System, Spinema Lumbar Plate System |
| Classification | Sacroiliac Joint Fixation |
| Applicant | Aegis Spine, Inc. 9781 S. Meridian Blvd, Ste 300 Englewood, CO 80112 |
| Contact | Kihyang Kim |
| Correspondent | Kihyang Kim Aegis Spine, Inc. 9781 S. Meridian Blvd, Ste 300 Englewood, CO 80112 |
| 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 | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-04-11 |
| Decision Date | 2022-06-30 |