The following data is part of a premarket notification filed by Zavation Medical Products Llc with the FDA for Normandy Vbr System.
Device ID | K180673 |
510k Number | K180673 |
Device Name: | Normandy VBR System |
Classification | Spinal Vertebral Body Replacement Device - Cervical |
Applicant | Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232 |
Contact | Frankie Cummins |
Correspondent | Frankie Cummins Zavation Medical Products LLC 220 Lakeland Parkway Flowood, MS 39232 |
Product Code | PLR |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-03-14 |
Decision Date | 2018-07-13 |
Summary: | summary |