KSEA SPINOSCOPE


Device Classification Name

arthroscope

510(k) Number K023187
Device Name KSEA SPINOSCOPE
Original Applicant
KARL STORZ ENDOSCOPY
600 corporate pointe
culver city, 
CA 
90230 -7600

Original Contact james a lee
Regulation Number 888.1100
Classification Product Code
HRX  
Date Received 09/24/2002
Decision Date 12/02/2002
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