FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Mazor X System / Mazor X Stealth Edition

K Number: K251316 · Decision Sep 11, 2025
Classifications
1
FEI Numbers
381
Registration Numbers
381
Same Product Code
430
Applicant Total
13
Review Days
135

Basic Information

Device Name
Mazor X System / Mazor X Stealth Edition
K Number
K251316
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mazor Robotics , Ltd.
Date Received
April 29, 2025
Decision Date
September 11, 2025
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

Other 510(k) clearances with the same product code (OLO), ordered by most recent decision date.

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Other Clearances by Mazor Robotics , Ltd.

K Number Device Name
K230064 Mazor X System (Mazor X Stealth Edition)
K203005 Mazor X
K200935 Mazor X
K182077 Mazor X System (Mazor X Stealth Edition)
K180307 Mazor X
K172522 Mazor X
K163221 Mazor X
K152041 Renaissance X System
K140167 RENAISSANCE X SYSTEM
K120812 RENAISSANCE
Search all 13 clearances from Mazor Robotics , Ltd. →