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 |