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

Camber Sacroiliac (SI) Fixation System

K Number: K233972 · Decision Feb 27, 2024
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
17
Review Days
74

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Basic Information

Device Name
Camber Sacroiliac (SI) Fixation System
K Number
K233972
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camber Spine Technologies
Date Received
December 15, 2023
Decision Date
February 27, 2024
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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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
K172446 SPIRA-C Open Matrix Cervical Interbody
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