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

Trigon Trigon HA Stand-Alone Wedge Fixation System

K Number: K234116 · Decision Jan 26, 2024
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
17
Applicant Total
4
Review Days
30

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Basic Information

Device Name
Trigon Trigon HA Stand-Alone Wedge Fixation System
K Number
K234116
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nvision Biomedical Technologies
Date Received
December 27, 2023
Decision Date
January 26, 2024
Product Code
PLF
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
PLF Bone Wedge

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Other Clearances by Nvision Biomedical Technologies

K Number Device Name
K250646 Impact PEEK Union Nail System
K242896 Caliber Intramedullary Fixation System
K243231 Trigon PEEK HA Wedges