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

EVOL® -SI Joint Fusion System

K Number: K190025 · Decision Aug 12, 2019
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
121
Applicant Total
10
Review Days
217

Basic Information

Device Name
EVOL® -SI Joint Fusion System
K Number
K190025
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
January 7, 2019
Decision Date
August 12, 2019
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

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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
K214123 T-FIX® 3DSI Joint Fusion System
K200991 EVOL Spinal Interbody System
K200552 EVOS Lumbar Interbody System
K192497 EVOL ha - D Lateral Interbody Fusion System
K180674 EVOL® ha-C Cervical Interbody Fusion System
K180891 EVOL Spinal Interbody System, EVOS Lumbar Interbody System
K150321 EVOS Lumbar Interbody System