Atlas FDA

Hexanium ACIF

FDA 510(k) clearance K221578 · decided 2022-11-14

Clearance details

K-number
K221578
Device name
Hexanium ACIF
Applicant
Spinevision, S.A.S.
Decision
Substantially Equivalent
Date received
2022-06-01
Decision date
2022-11-14
Days to decision
166 days
Clearance type
Special
Product code
OVE
Device class
2
Regulation number
888.3080
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Antony, FR
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.