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

Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft

K Number: K191696 · Decision Dec 27, 2019
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
0
Applicant Total
16
Review Days
185

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Basic Information

Device Name
Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft
K Number
K191696
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 Incorporated
Date Received
June 25, 2019
Decision Date
December 27, 2019
Product Code
OXN
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
OXN Mesh, Surgical, Collagen, Fistula

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
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
K160136 Flowable Wound Matrix
K161221 Biodesign Sling, Biodesign Plastic Surgery Matrix, Biodesign Anal Fistula Plug
Search all 16 clearances from Cook Biotech Incorporated →