FDA 510(k) Application Details - K202393

Device Classification Name	Cement, Bone, Vertebroplasty   More FDA Info for this Device
510(K) Number	K202393
Device Name	Cement, Bone, Vertebroplasty
Applicant	Stryker Corporation 1926 Stryker Way Kalamazoo, MI 49002 US Other 510(k) Applications for this Company
Contact	Kristi Ashton Other 510(k) Applications for this Contact
Regulation Number	888.3027   More FDA Info for this Regulation Number
Classification Product Code	NDN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/21/2020
Decision Date	10/20/2020
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