The following data is part of a premarket notification filed by Wishbone Medical, Inc. with the FDA for Wishbone Medical Plate And Screw System.
Device ID | K180736 |
510k Number | K180736 |
Device Name: | WishBone Medical Plate And Screw System |
Classification | Plate, Fixation, Bone |
Applicant | WishBone Medical, Inc. 1250 North Pointe Drive Warsaw, IN 46992 |
Contact | Gary Barnett |
Correspondent | Gary Barnett WishBone Medical, Inc. 1250 North Pointe Drive Warsaw, IN 46992 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-03-22 |
Decision Date | 2018-10-04 |