FDA 510(k) Application Details - K232394

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K232394
Device Name	Plate, Fixation, Bone
Applicant	Changzhou Geasure Medical Apparatus and Instruments Co., Ltd No. 12, Jinfeng Road, West Taihu Science and Technology Industrial Park Changzhou 213149 CN Other 510(k) Applications for this Company
Contact	Jing Huang Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	HRS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/09/2023
Decision Date	12/15/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review