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

BOSS Toe Fixation System

K Number: K190261 · Decision Aug 14, 2019
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
26
Review Days
187

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Basic Information

Device Name
BOSS Toe Fixation System
K Number
K190261
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3730
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Arthrosurface, Inc.
Date Received
February 8, 2019
Decision Date
August 14, 2019
Product Code
KWD
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
KWD Prosthesis, Toe, Hemi-, Phalangeal

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