The following data is part of a premarket notification filed by Wishbone Medical with the FDA for Wishbone Guided Growth System.
Device ID | K182704 |
510k Number | K182704 |
Device Name: | WishBone Guided Growth System |
Classification | Plate, Bone, Growth Control, Pediatric, Epiphysiodesis |
Applicant | WishBone Medical 1250 North Pointe Drive Warsaw, IN 46992 |
Contact | Gary Barnett |
Correspondent | Mary Wetzel WishBone Medical 2150 North Pointe Drive Warsaw, IN 46582 |
Product Code | OBT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-09-27 |
Decision Date | 2019-06-25 |