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 |