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

SURGISIS STAPLE LINE REINFORCEMENT II

K Number: K051048 · Decision Sep 23, 2005
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
162
Applicant Total
31
Review Days
151

Basic Information

Device Name
SURGISIS STAPLE LINE REINFORCEMENT II
K Number
K051048
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
COOK BIOTECH, INC.
Date Received
April 25, 2005
Decision Date
September 23, 2005
Product Code
FTM
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
FTM Mesh, Surgical

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K Number Device Name
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K111695 HYBRID GRAFT
K110402 BIODESIGN NIPPLE RECONSTRUCTION CYLINDER
K090688 COOK UROLOGICAL GRAFT
K082682 SURGISIS BIODESIGN ENTEROCUTANEOUS FISTULA PLUG
K082058 DYNAMATRIX
K073391 SURGISIS BIODESIGN TISSUE GRAFT
K070405 MODIFICATION TO SURGISIS SLR STAPLE LINE REINFORCEMENT
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