Atlas FDA

NextAR Hip Platform

FDA 510(k) clearance K252847 · decided 2026-01-09

Clearance details

K-number
K252847
Device name
NextAR Hip Platform
Applicant
Medacta International S.A.
Decision
Substantially Equivalent
Date received
2025-09-08
Decision date
2026-01-09
Days to decision
123 days
Clearance type
Traditional
Product code
SBF
Device class
2
Regulation number
882.4560
Medical specialty
Neurology
Advisory committee
Neurology
Location
Castel San Pietro, CH
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.