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

CORUS™ Navigation System-GN

K Number: K261665 · Decision Jun 18, 2026
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
21
Review Days
29

Basic Information

Device Name
CORUS™ Navigation System-GN
K Number
K261665
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Providence Medical Technology, Inc.
Date Received
May 20, 2026
Decision Date
June 18, 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

Similar 510(k) Clearances

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Other Clearances by Providence Medical Technology, Inc.

K Number Device Name
K253676 CORUS™ Posterior Cervical Stabilization System 3D (CORUS™ PCSS 3D)
K253190 CORUS-LX Implant
K251060 CORUS™ Navigation System-GX
K251885 CAVUX Facet Fixation System (CAVUX FFS) and CORUS-LX Implant
K241035 PMT Posterior Cervical Stabilization System (PCSS)
K240625 CORUS Navigation Access System
K230840 PMT Facet Fixation System, Lumbar (PMT FFS-LX)
K230297 PMT Expandable Cage (PMT EXP)
K220951 PMT Facet Fixation System (PMT FFS)
K212636 CORUS Spinal System-X
Search all 21 clearances from Providence Medical Technology, Inc. →