FDA 510(k) Application Details - K955229

Device Classification Name	Blade, Saw, General & Plastic Surgery, Surgical   More FDA Info for this Device
510(K) Number	K955229
Device Name	Blade, Saw, General & Plastic Surgery, Surgical
Applicant	WRIGHT MEDICAL TECHNOLOGY, INC. 5677 AIRLINE RD. ARLINGTON, TN 38002 US Other 510(k) Applications for this Company
Contact	CRISTIE MANUEL Other 510(k) Applications for this Contact
Regulation Number	878.4820   More FDA Info for this Regulation Number
Classification Product Code	GFA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/14/1995
Decision Date	01/18/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review