FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Robotic Integration Instruments

K Number: K233256 · Decision Jun 17, 2024
Classifications
1
FEI Numbers
370
Registration Numbers
370
Same Product Code
404
Applicant Total
14
Review Days
263

Basic Information

Device Name
Robotic Integration Instruments
K Number
K233256
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DePuy Synthes
Date Received
September 28, 2023
Decision Date
June 17, 2024
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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