FDA 510(k) Application Details - K230908

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K230908
Device Name	Screw, Fixation, Bone
Applicant	Skeletal Dynamics, Inc. 7300 North Kendall Drive Suite 400 Miami, FL 33156 US Other 510(k) Applications for this Company
Contact	Alexandra Rodriguez Rojas Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/31/2023
Decision Date	04/28/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review