The following data is part of a premarket notification filed by Zavation, Llc with the FDA for Zavation Spinal System.
Device ID | K153404 |
510k Number | K153404 |
Device Name: | Zavation Spinal System |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | ZAVATION, LLC 400 LIBERTY PARK DR Flowood, MS 39232 |
Contact | Lawrence Walker |
Correspondent | Lawrence Walker ZAVATION, LLC 400 LIBERTY PARK DR Flowood, MS 39232 |
Product Code | MNH |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-11-24 |
Decision Date | 2016-04-21 |
Summary: | summary |