The following data is part of a premarket notification filed by Benvenue Medical, Inc. with the FDA for Kiva Vcf Treatment System.
| Device ID | K141141 |
| 510k Number | K141141 |
| Device Name: | KIVA VCF TREATMENT SYSTEM |
| Classification | Cement, Bone, Vertebroplasty |
| Applicant | BENVENUE MEDICAL, INC. 1171 BARROILHET DR. Hillsborough, CA 94010 |
| Contact | Cindy Domecus, R.a.c. |
| Correspondent | Cindy Domecus, R.a.c. BENVENUE MEDICAL, INC. 1171 BARROILHET DR. Hillsborough, CA 94010 |
| Product Code | NDN |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-05-02 |
| Decision Date | 2014-08-14 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00815212024450 | K141141 | 000 |
| 00815212024443 | K141141 | 000 |
| 00815212023606 | K141141 | 000 |
| 00815212023590 | K141141 | 000 |
| 00815212023514 | K141141 | 000 |
| 00815212023507 | K141141 | 000 |
| 00815212023491 | K141141 | 000 |
| 00815212023484 | K141141 | 000 |