ZIMMER MIS LIGHT


Device Classification Name

light, surgical, fiberoptic

510(k) Number K080367
Device Name ZIMMER MIS LIGHT
Applicant
ZIMMER SPINE, INC.
7375 bush lake rd.
minneapolis, 
MN 
55439

Applicant Contact elsa a linke
Correspondent
ZIMMER SPINE, INC.
7375 bush lake rd.
minneapolis, 
MN 
55439

Correspodent Contact elsa a linke
Regulation Number 878.4580
Classification Product Code
FST  
Date Received 02/12/2008
Decision Date 02/22/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No