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

SMITH & NEPHEW INSTRUMENT TRAYS

K Number: K091627 · Decision Jul 2, 2009
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
529
Review Days
29

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Basic Information

Device Name
SMITH & NEPHEW INSTRUMENT TRAYS
K Number
K091627
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith & Nephew, Inc.
Date Received
June 3, 2009
Decision Date
July 2, 2009
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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K254084 AETOS Shoulder System - CONCELOC Glenoids
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K251627 BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid blue); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (white); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid blue)
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)
Search all 529 clearances from Smith & Nephew, Inc. →