FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUPRAMESH EXTRA

K Number: K080216 · Decision Sep 15, 2008
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
16
Review Days
230

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Basic Information

Device Name
SUPRAMESH EXTRA
K Number
K080216
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
S. Jackson, Inc.
Date Received
January 29, 2008
Decision Date
September 15, 2008
Product Code
FTL
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FTL Mesh, Surgical, Polymeric

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FTL), ordered by most recent decision date.

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Other Clearances by S. Jackson, Inc.

K Number Device Name
K973379 STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS
K931614 MOPYLEN SUTURE
K931613 SUPRAMID SUTURE
K931612 NYLAMID SUTURE
K922630 MOPYLEN
K912429 N80-838 SUPRAMID EXTRA SUTURE
K904052 SUPRAMID EXTRA SUTURES
K852011 NYLAMID MESH PAD FULL & HALF
K831725 FOIL IN 3 FORMS-NON-STERILE SHEETS
K831727 QUARTER GLOBE CAPS
Search all 16 clearances from S. Jackson, Inc. →