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

MOPYLEN SUTURE

K Number: K931614 · Decision Dec 17, 1993
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
16
Review Days
260

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Basic Information

Device Name
MOPYLEN SUTURE
K Number
K931614
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.5010
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
S. Jackson, Inc.
Date Received
April 1, 1993
Decision Date
December 17, 1993
Product Code
GAW
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
GAW Suture, Nonabsorbable, Synthetic, Polypropylene

Similar 510(k) Clearances

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

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Other Clearances by S. Jackson, Inc.

K Number Device Name
K080216 SUPRAMESH EXTRA
K973379 STERILE SUPRAFOIL SMOOTH NYLON FOIL SHEETS
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. →