The following data is part of a premarket notification filed by Tianjin Walkman Biomaterial Co., Ltd. with the FDA for Metallic Locking Compression Bone Plates And Screws System.
Device ID | K131759 |
510k Number | K131759 |
Device Name: | METALLIC LOCKING COMPRESSION BONE PLATES AND SCREWS SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | TIANJIN WALKMAN BIOMATERIAL CO., LTD. P.O. BOX 120-119 Shanghai, CN 200120 |
Contact | Diana Hong |
Correspondent | Diana Hong TIANJIN WALKMAN BIOMATERIAL CO., LTD. P.O. BOX 120-119 Shanghai, CN 200120 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-17 |
Decision Date | 2013-08-08 |
Summary: | summary |