FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SS MATRIX

K Number: K020732 · Decision May 30, 2002
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
31
Review Days
85

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Basic Information

Device Name
SS MATRIX
K Number
K020732
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Biotech, Inc.
Date Received
March 6, 2002
Decision Date
May 30, 2002
Product Code
KGN
Advisory Committee
Unknown
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
KGN Wound Dressing With Animal-Derived Material(S)

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Other Clearances by Cook Biotech, Inc.

K Number Device Name
K133306 SIS HERNIA GRAFT
K133011 DIAPHRAGMATIC HERNIA GRAFT
K131015 BIODESIGN ONLAY DURAL GRAFT OR BIODESIGN DURAPLASTY GRAFT
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
Search all 31 clearances from Cook Biotech, Inc. →