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

Cervical Stand-Alone System

K Number: K212853 · Decision Nov 5, 2021
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
161
Applicant Total
4
Review Days
59

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Basic Information

Device Name
Cervical Stand-Alone System
K Number
K212853
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, LLC
Date Received
September 7, 2021
Decision Date
November 5, 2021
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Similar 510(k) Clearances

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Other Clearances by Eminent Spine, LLC

K Number Device Name
K240505 Eminent Spine SI Screw System
K230219 Eminent Spine 3D Lumbar Interbody Fusion Systems
K201979 Cervical Plate System