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

Navigated LLIF Impactable Tracker

K Number: K261060 · Decision May 29, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
31
Review Days
59

Basic Information

Device Name
Navigated LLIF Impactable Tracker
K Number
K261060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tyber Medical, LLC
Date Received
March 31, 2026
Decision Date
May 29, 2026
Product Code
OLO
Advisory Committee
Neurology
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
OLO Orthopedic Stereotaxic Instrument

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K Number Device Name
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K252742 Navigated Instruments
K251361 Tyber Medical Distal Radius Plating System
K242486 Tyber Medical Anatomical Plating System
K241218 Tyber Medical Anatomical Plating System
K233423 Tyber Medical Anatomical Plating System – Line extension to the Mini-Frag System
K233017 TM Plating System
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