INTERPORE CROSS CEMENT RESTRICTOR


Device Classification Name

prosthesis, hip, cement restrictor

510(k) Number K023908
Device Name INTERPORE CROSS CEMENT RESTRICTOR
Original Applicant
INTERPORE CROSS INTL.
181 technology dr.
irvine, 
CA 
92618 -2402

Original Contact prosie rey-fessler
Regulation Number 878.3300
Classification Product Code
JDK  
Date Received 11/25/2002
Decision Date 05/16/2003
Decision

se – with limitations

(SESU)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No