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

T-FIX® 3DSI Joint Fusion System

K Number: K214123 · Decision Jun 24, 2022
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
11
Review Days
176

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Basic Information

Device Name
T-FIX® 3DSI Joint Fusion System
K Number
K214123
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cutting Edge Spine, LLC
Date Received
December 30, 2021
Decision Date
June 24, 2022
Product Code
OUR
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
OUR Sacroiliac Joint Fixation

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OUR), ordered by most recent decision date.

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Other Clearances by Cutting Edge Spine, LLC

K Number Device Name
K250605 EVOL® ha – Hyper C Cervical Interbody Fusion System
K230689 T-FIX™ 3DSI Joint Fusion System
K200991 EVOL Spinal Interbody System
K200552 EVOS Lumbar Interbody System
K192497 EVOL ha - D Lateral Interbody Fusion System
K190025 EVOL® -SI Joint Fusion System
K180674 EVOL® ha-C Cervical Interbody Fusion System
K180891 EVOL Spinal Interbody System, EVOS Lumbar Interbody System
K150321 EVOS Lumbar Interbody System
K102957 CUTTING EDGE SPINE INTERBODY FUSION DEVICE
Search all 11 clearances from Cutting Edge Spine, LLC →