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

Stryker ICONIX with Needles

K Number: K151201 · Decision Jun 29, 2015
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
92
Review Days
55

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Basic Information

Device Name
Stryker ICONIX with Needles
K Number
K151201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker
Date Received
May 5, 2015
Decision Date
June 29, 2015
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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