IndexMethodologyInsightsFor CliniciansRequest Review
Index/Elekta Instrument AB
ALT-001401K013861Amber Status

Elekta Instrument AB

MODIFICATION TO LEKSELL SURGIPLAN WITH ATLASPACE

All identifiers (2)
Aletia (canonical)ALT-001401
FDA 510(k) ยท US (primary)K013861

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K013861
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
Some fields are incomplete or unverified. If you represent Elekta Instrument AB, you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index