SUPRAMID EXTRA SURGICAL MESH

Mesh, Surgical

S. JACKSON, INC.

The following data is part of a premarket notification filed by S. Jackson, Inc. with the FDA for Supramid Extra Surgical Mesh.

Pre-market Notification Details

Device IDK831723
510k NumberK831723
Device Name:SUPRAMID EXTRA SURGICAL MESH
ClassificationMesh, Surgical
Applicant S. JACKSON, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFTM  
CFR Regulation Number878.3300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-05-31
Decision Date1983-08-12

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