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 |