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

Flowable Wound Matrix

K Number: K160136 · Decision Sep 28, 2016
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
16
Review Days
252

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Basic Information

Device Name
Flowable Wound Matrix
K Number
K160136
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Biotech Incorporated
Date Received
January 20, 2016
Decision Date
September 28, 2016
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 Incorporated

K Number Device Name
K232646 Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.6-0.9)
K201000 Biodesign Staple Line Reinforcement
K191696 Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft
K171817 Biodesign Diaphragmatic Hernia Graft
K162934 Biodesign Parastomal Hernia Repair Graft
K170016 Biodesign Fistula Plug
K170945 Biodesign Staple Line Reinforcement
K161762 DynaMatrix/Dynamatrix Plus
K162741 AxoGuard Nerve Connector
K161221 Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
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