LigaPASS™ 2.0 Ligament Augmentation System— 510(k) K213659

Substantially Equivalent

Medicrea International SA

FDA 510(k) clearance K213659 for LigaPASS™ 2.0 Ligament Augmentation System, Substantially Equivalent on 2022-05-24. Applicant: Medicrea International SA.

Clearance details

Applicant
Medicrea International SA
Product code
Code OWI
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Rillieux-La-Pape, FR
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Data sourced from openFDA. This site is unofficial and independent of the FDA.