MASTERGRAFT MATRIX


Device Classification Name

filler, bone void, calcium compound

510(k) Number K023553
Device Name MASTERGRAFT MATRIX
Original Applicant
MEDTRONIC SOFAMOR DANEK, INC.
1800 pyramid place
memphis, 
TN 
38132

Original Contact richard w treharne
Regulation Number 888.3045
Classification Product Code
MQV  
Date Received 10/23/2002
Decision Date 04/22/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No