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 |