FDA 510(k) Application Details - K232350

Device Classification Name	Plate, Bone   More FDA Info for this Device
510(K) Number	K232350
Device Name	Plate, Bone
Applicant	Stryker Craniomaxillofacial 1941 Stryker Way Portage, MI 49002 US Other 510(k) Applications for this Company
Contact	Jonathan Schell Other 510(k) Applications for this Contact
Regulation Number	872.4760   More FDA Info for this Regulation Number
Classification Product Code	JEY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/07/2023
Decision Date	01/13/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review