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

Vector Hammertoe Correction System

K Number: K183055 · Decision Feb 19, 2019
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
10
Review Days
109

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Basic Information

Device Name
Vector Hammertoe Correction System
K Number
K183055
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nvision Biomedical Technologies, LLC
Date Received
November 2, 2018
Decision Date
February 19, 2019
Product Code
HWC
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
HWC Screw, Fixation, Bone

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