The following data is part of a premarket notification filed by Shanghai Kinetic Medical Co., Ltd with the FDA for Kmc Kyphoplasty System.
| Device ID | K113742 |
| 510k Number | K113742 |
| Device Name: | KMC KYPHOPLASTY SYSTEM |
| Classification | Cement, Bone, Vertebroplasty |
| Applicant | SHANGHAI KINETIC MEDICAL CO., LTD 3924CASCADE BEACH ROAD Lutsen, MN 55612 |
| Contact | Gregory Mathison |
| Correspondent | Gregory Mathison SHANGHAI KINETIC MEDICAL CO., LTD 3924CASCADE BEACH ROAD Lutsen, MN 55612 |
| Product Code | NDN |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-12-20 |
| Decision Date | 2012-09-17 |
| Summary: | summary |