The following data is part of a premarket notification filed by Wishbone Medical, Inc. with the FDA for Smart Correction System Rings And Compatible Ha-coated Half Pins.
Device ID | K221366 |
510k Number | K221366 |
Device Name: | Smart Correction System Rings And Compatible HA-Coated Half Pins |
Classification | Appliance, Fixation, Nail/blade/plate Combination, Multiple Component |
Applicant | WishBone Medical, Inc. 100 Capital Drive Warsaw, IN 46582 |
Contact | Ramakrishna Bajaj |
Correspondent | Kellie Myers WishBone Medical, Inc. 100 Capital Drive Warsaw, IN 46582 |
Product Code | KTT |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-05-12 |
Decision Date | 2022-06-06 |