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

iFuse Implant System®

K Number: K190230 · Decision Apr 3, 2019
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
130
Applicant Total
32
Review Days
56

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Basic Information

Device Name
iFuse Implant System®
K Number
K190230
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SI-BONE, Inc.
Date Received
February 6, 2019
Decision Date
April 3, 2019
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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Other Clearances by SI-BONE, Inc.

K Number Device Name
K253488 iFuse INTRA Ti™ Implant System
K253094 iFuse Bedrock Granite Implant System
K251780 iGPS Navigation Instruments
K241504 iFuse TORQ TNT™ Implant System
K241574 iFuse TORQ® Implant System
K232800 Navigation Tracking Instruments
K233508 iFuse Bedrock Granite® Implant System
K231689 iFuse TORQ® Implant System
K222774 iFuse Bedrock Granite® Implant System
K222605 iFuse TORQ® Implant System
Search all 32 clearances from SI-BONE, Inc. →