The following data is part of a premarket notification filed by Weigao Orthopaedic Device Co., Ltd with the FDA for Locking Bone Plates And Screws.
| Device ID | K130340 |
| 510k Number | K130340 |
| Device Name: | LOCKING BONE PLATES AND SCREWS |
| Classification | Plate, Fixation, Bone |
| Applicant | WEIGAO ORTHOPAEDIC DEVICE CO., LTD PO BOX 237-023 Shanghai, CN 200237 |
| Contact | Diana Hong |
| Correspondent | Diana Hong WEIGAO ORTHOPAEDIC DEVICE CO., LTD PO BOX 237-023 Shanghai, CN 200237 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-02-11 |
| Decision Date | 2013-04-05 |
| Summary: | summary |