ALT-001552K031980Amber Status
Elekta Instrument AB
MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001552FDA 510(k) · US (primary)
K031980Regulatory Registrations
🌐
US
FDA
ID: K031980
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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