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

ICONIX TT All Suture Anchor

K Number: K170098 · Decision Mar 31, 2017
Classifications
1
FEI Numbers
263
Registration Numbers
263
Same Product Code
564
Applicant Total
86
Review Days
79

Basic Information

Device Name
ICONIX TT All Suture Anchor
K Number
K170098
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker
Date Received
January 11, 2017
Decision Date
March 31, 2017
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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