FDA 510(k) Application Details - K240958

Device Classification Name	Plate, Fixation, Bone   More FDA Info for this Device
510(K) Number	K240958
Device Name	Plate, Fixation, Bone
Applicant	Hebei Ruihe Medical Devices Co., Ltd. No. 599 Qinling St, High-tech Industrial Development Zone Shijiazhuang 051430 CN Other 510(k) Applications for this Company
Contact	Mengjia Chi 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	04/08/2024
Decision Date	02/10/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review