The following data is part of a premarket notification filed by Zavation Medical Products, Llc with the FDA for Zavation Varisync Plate System And Varisync Spacer System.
| Device ID | K221049 |
| 510k Number | K221049 |
| Device Name: | Zavation VariSync Plate System And VariSync Spacer System |
| Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
| Applicant | Zavation Medical Products, LLC 220 Lakeland Parkway Flowood, MS 39232 |
| Contact | Katie Motley |
| Correspondent | Katie Motley Zavation Medical Products, LLC 3670 Flowood Drive Flowood, MS 39232 |
| Product Code | OVE |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | ODP |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-04-11 |
| Decision Date | 2022-08-12 |