ALT-001395K013569Amber Status
Aesculap, Inc.
ORTHOPILOT 2
All identifiers (2)
Aletia (canonical)
ALT-001395FDA 510(k) · US (primary)
K013569Regulatory Registrations
🌐
US
FDA
ID: K013569
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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