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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name mesh, surgical, synthetic, urogynecologic, for stress urinary incontinence, female, mini-sling
510(k) Number K020652
Device Name HERNIAMESH T-SLING
Applicant
HERNIAMESH
8 ORANGE DR.
JERICHO,  NY  11753
Applicant Contact LORENA TRABUCCO
Correspondent
HERNIAMESH
8 ORANGE DR.
JERICHO,  NY  11753
Correspondent Contact LORENA TRABUCCO
Regulation Number878.3300
Classification Product Code
PAH  
Date Received02/28/2002
Decision Date 05/15/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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