CRYOMINI


Device Classification Name

powered laser surgical instrument

510(k) Number K080735
Device Name CRYOMINI
Applicant
ZIMMER ELEKTROMEDIZIN GMBH
junkersstrasse 9
neu-ulm, 

DE

89231

Applicant Contact armin petraschka
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 03/17/2008
Decision Date 04/04/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Special
Reviewed by Third Party Yes

Combination Product

No