FDA 510(k) Application Details - K092721

Device Classification Name	Prosthesis, Elbow, Hemi-, Radial, Polymer   More FDA Info for this Device
510(K) Number	K092721
Device Name	Prosthesis, Elbow, Hemi-, Radial, Polymer
Applicant	SKELETAL DYNAMICS, LLC 80 SHELDON TECHNOLOGY CENTER SHELTON, CT 06484 US Other 510(k) Applications for this Company
Contact	JOSEPH AZARY Other 510(k) Applications for this Contact
Regulation Number	888.3170   More FDA Info for this Regulation Number
Classification Product Code	KWI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/04/2009
Decision Date	08/03/2010
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