VENTRAL WALL DEFECT REDUCT SILO

Mesh, Surgical, Polymeric

AMERICAN HEYER SCHULTE

The following data is part of a premarket notification filed by American Heyer Schulte with the FDA for Ventral Wall Defect Reduct Silo.

Pre-market Notification Details

• Device ID: K840172
• 510k Number: K840172
• Device Name: VENTRAL WALL DEFECT REDUCT SILO
• Classification: Mesh, Surgical, Polymeric
• Applicant: AMERICAN HEYER SCHULTE 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: FTL
• CFR Regulation Number: 878.3300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-01-17
• Decision Date: 1984-06-27

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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