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

SMITH & NEPHEW ULTRABRAID SUTURE

K Number: K041216 · Decision Jun 7, 2004
Classifications
1
FEI Numbers
242
Registration Numbers
242
Same Product Code
173
Applicant Total
529
Review Days
28

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Basic Information

Device Name
SMITH & NEPHEW ULTRABRAID SUTURE
K Number
K041216
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
878.5000
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew, Inc.
Date Received
May 10, 2004
Decision Date
June 7, 2004
Product Code
GAT
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
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

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K243608 TRIGEN Stable Lock Nut & Washer
K250677 LEGION Total Knee System
K250571 CATALYSTEM Femoral Stems
K243364 TRIGEN META-TAN Trochanteric Antegrade Nail
K240716 AETOS Shoulder System Stemless Humeral Prosthesis
K242711 JOURNEY II Unicompartmental Knee System (JOURNEY II UK)
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