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

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage

K Number: K173800 · Decision Feb 2, 2018
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
17
Review Days
50

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Basic Information

Device Name
Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage
K Number
K173800
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camber Spine Technologies
Date Received
December 14, 2017
Decision Date
February 2, 2018
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

Similar 510(k) Clearances

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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
K172446 SPIRA-C Open Matrix Cervical Interbody
Search all 17 clearances from Camber Spine Technologies →