The following data is part of a premarket notification filed by Zavation Llc with the FDA for Zvplasty.
Device ID | K141419 |
510k Number | K141419 |
Device Name: | ZVPLASTY |
Classification | Cement, Bone, Vertebroplasty |
Applicant | ZAVATION LLC 400 LIBERTY PARK DR Flowood, MS 39232 |
Contact | John Walker |
Correspondent | John Walker ZAVATION LLC 400 LIBERTY PARK DR Flowood, MS 39232 |
Product Code | NDN |
Subsequent Product Code | GAA |
Subsequent Product Code | HRX |
CFR Regulation Number | 888.3027 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-05-29 |
Decision Date | 2014-09-12 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZVPLASTY 86292350 4814004 Live/Registered |
ZAVATION MEDICAL PRODUCTS LLC 2014-05-27 |