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

Biodesign Otologic Repair Graft

K Number: K161000 · Decision May 11, 2016
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
32
Applicant Total
16
Review Days
30

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Basic Information

Device Name
Biodesign Otologic Repair Graft
K Number
K161000
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Biotech Incorporated
Date Received
April 11, 2016
Decision Date
May 11, 2016
Product Code
KHJ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)

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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
K160136 Flowable Wound Matrix
Search all 16 clearances from Cook Biotech Incorporated →