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 |