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

ENZA Zero-Profile Anterior Interbody Fusion

K Number: K153720 · Decision May 3, 2016
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
17
Review Days
127

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Basic Information

Device Name
ENZA Zero-Profile Anterior Interbody Fusion
K Number
K153720
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camber Spine Technologies
Date Received
December 28, 2015
Decision Date
May 3, 2016
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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Other Clearances by Camber Spine Technologies

K Number Device Name
K234077 SPIRA® Anterior Lumbar Spacers
K233972 Camber Sacroiliac (SI) Fixation System
K230942 SPIRA® Posterior Lumbar Spacers
K221324 ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)
K223837 SPIRA®-C Integrated Fixation System
K220038 Camber Spine Navigation System
K193153 SPIRA-C Integrated Fixation System
K190483 SPIRA Open Matrix ALIF and LLIF
K173432 ENZA-A Titanium ALIF
K173800 Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage
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