FDA 510(k) Application Details - K182425

Device Classification Name	Plate, Cranioplasty, Preformed, Alterable   More FDA Info for this Device
510(K) Number	K182425
Device Name	Plate, Cranioplasty, Preformed, Alterable
Applicant	Stryker Leibinger GmbH & Co. KG Boetzinger Strasse 41 Freiburg D-79111 DE Other 510(k) Applications for this Company
Contact	Gregory Gohl Other 510(k) Applications for this Contact
Regulation Number	882.5320   More FDA Info for this Regulation Number
Classification Product Code	GWO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/06/2018
Decision Date	11/06/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review