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

Standalone ALIF Interbody Fusion System

K Number: K221936 · Decision Oct 17, 2022
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
11
Review Days
108

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Basic Information

Device Name
Standalone ALIF Interbody Fusion System
K Number
K221936
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Eminent Spine
Date Received
July 1, 2022
Decision Date
October 17, 2022
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

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K212701 Eminent Spine 3D Cervical Interbody Fusion System
K143365 Eminent Foot Plate System
K133194 DIAMOND RATTLESNAKE SYSTEM
K103068 KING COBRA ANTERIOR CERVICAL PLATE
K100377 DIAMONDBACK SPINAL SYSTEM
K090415 EMINENT SPINE BUTTRESS (FANG) PLATE SYSTEM
K090064 EMINENT SPINE INTERBODY FUSION SYSTEM
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