510(k) K240872

Device
Erisma® Deformity Spinal System; Erisma® Lp Spinal Fixation System
Applicant
Clariance
510(k) number
K240872
Product code
NKB
Decision
Substantially Equivalent (SESE)
Decision date
2024-04-26
Date received
2024-03-29
Regulation
888.3070
Classification name
Thoracolumbosacral Pedicle Screw System
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Magalie Hennequin
Address
18, Rue Robespierre Beaurains FR 62217 62217

FDA Registration Numbers

Source Documents

510(k) summary PDF

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