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

Argo Knotless GENESYS Anchor

K Number: K240090 · Decision Mar 5, 2024
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
82
Review Days
53

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Basic Information

Device Name
Argo Knotless GENESYS Anchor
K Number
K240090
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Conmed Corporation
Date Received
January 12, 2024
Decision Date
March 5, 2024
Product Code
MAI
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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