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

UNITY Sacroiliac Joint Fixation System

K Number: K222448 · Decision Oct 13, 2022
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
4
Review Days
59

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Basic Information

Device Name
UNITY Sacroiliac Joint Fixation System
K Number
K222448
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dio Medical Corporation
Date Received
August 15, 2022
Decision Date
October 13, 2022
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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