ALT-001902K062358Amber Status
Brainlab AG
MODIFICATION TO VECTORVISION TRAUMA
All identifiers (2)
Aletia (canonical)
ALT-001902FDA 510(k) ยท US (primary)
K062358Regulatory Registrations
๐
US
FDA
ID: K062358
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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Some fields are incomplete or unverified. If you represent Brainlab AG, you can verify and update this listing.
