510(k) K221578

Device
Hexanium ACIF
Applicant
Spinevision, S.A.S.
510(k) number
K221578
Product code
OVE
Decision
Substantially Equivalent (SESE)
Decision date
2022-11-14
Date received
2022-06-01
Regulation
888.3080
Classification name
Intervertebral Fusion Device With Integrated Fixation, Cervical
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Quang Tran
Address
10 Rue De La Renaissance Antony FR 92160 92160

FDA Registration Numbers

Source Documents

510(k) summary PDF

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