FDA 510(k) Application Details - K970273

Device Classification Name	Restraint, Protective   More FDA Info for this Device
510(K) Number	K970273
Device Name	Restraint, Protective
Applicant	FLA. ORTHOPEDICS, INC. 5757 NW 158TH ST. MIAMI LAKES, FL 33014 US Other 510(k) Applications for this Company
Contact	RHONDA FALK Other 510(k) Applications for this Contact
Regulation Number	880.6760   More FDA Info for this Regulation Number
Classification Product Code	FMQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/23/1997
Decision Date	04/11/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review