FDA 510(k) Application Details - K193451

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K193451
Device Name	Screw, Fixation, Bone
Applicant	Biomet Inc. 56 East Bell Drive, PO Box 587 Warsaw, IN 46581 US Other 510(k) Applications for this Company
Contact	Saveetha Raghupathi 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	12/13/2019
Decision Date	02/24/2020
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