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 |