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Rt Elements, Dose Review, Brain Metastases, Adaptive Hybrid Surgery Analysis

FDA 510(k)

Class II (US FDA 510(k))

510(k) K142108

by Brainlab AG

Identifiers

510(k) Number
K142108 FDA 510(k)
FDA Product Code
MUJ FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 892.5050 FDA 510(k)
Regulation Number
892.5050 FDA 510(k)
Advisory Committee
Radiology FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Rt Elements, Dose Review, Brain Metastases, Adaptive Hybrid Surgery Analysis by Brainlab AG — Class II — FDA_510K — listed in FDA 510(k)

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Brainlab AG

Sources (1)

  • FDA 510(k) K142108 24 fields · synced Jun 18, 2026