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

MICRORAPTOR Knotless Suture Anchor

K Number: K181746 · Decision Sep 28, 2018
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
7
Review Days
88

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Basic Information

Device Name
MICRORAPTOR Knotless Suture Anchor
K Number
K181746
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Smith and Nephew, Inc.
Date Received
July 2, 2018
Decision Date
September 28, 2018
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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K191177 LENS 4K Camera Control Unit - Wifi, LENS 4K Camera Control Unit - Non-Wifi, LENS 4K Camera Head
K183232 Double ENDOBUTTON Fixation Device
K180361 MICRORAPTOR REGENESORB Suture Anchor
K163034 SUTUREFIX Curved Suture Anchor