OSTEOPLAST, MODEL POP200


Device Classification Name

filler, bone void, calcium compound

510(k) Number K991854
Device Name OSTEOPLAST, MODEL POP200
Applicant
INTERPORE CROSS INTL.
181 technology dr.
irvine, 
CA 
92618 -2402

Applicant Contact lynn rodarti
Correspondent
INTERPORE CROSS INTL.
181 technology dr.
irvine, 
CA 
92618 -2402

Correspodent Contact lynn rodarti
Regulation Number 888.3045
Classification Product Code
MQV  
Date Received 06/01/1999
Decision Date 08/26/1999
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