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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name barrier, synthetic, intraoral
510(k) Number K960292
Device Name GORE-TEX REGENERATIVE MATERIAL TITANIUM REINFORCED CONFIGURATIONS
Applicant
W.L. GORE & ASSOCIATES,INC
1500 NORTH FOURTH ST.
FLAGSTAFF,  AZ  86001
Applicant Contact JACQUELINE KALBACH
Correspondent
W.L. GORE & ASSOCIATES,INC
1500 NORTH FOURTH ST.
FLAGSTAFF,  AZ  86001
Correspondent Contact JACQUELINE KALBACH
Regulation Number872.3930
Classification Product Code
NPK  
Date Received01/22/1996
Decision Date 04/15/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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