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

Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.6-0.9)

K Number: K232646 · Decision May 24, 2024
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
32
Applicant Total
16
Review Days
268

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Basic Information

Device Name
Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.4-0.6); Biodesign Otologic Butterfly Graft (ENT-OTO-BFLY-0.6-0.9)
K Number
K232646
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cook Biotech Incorporated
Date Received
August 30, 2023
Decision Date
May 24, 2024
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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K Number Device Name
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K162934 Biodesign Parastomal Hernia Repair Graft
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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
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