PROPLATE


Device Classification Name

electrosurgical, cutting & coagulation & accessories

510(k) Number K073360
Device Name PROPLATE
Applicant
BIO PROTECH, INC.
1676 village green suite a
crofton, 
MD 
21114

Applicant Contact e.j. smith
Regulation Number 878.4400
Classification Product Code
GEI  
Date Received 11/30/2007
Decision Date 12/19/2007
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No