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FDA 510(k) Application Details - K202032
Device Classification Name
More FDA Info for this Device
510(K) Number
K202032
Device Name
Idys LLIF 3DTi
Applicant
Clariance, SAS
18, rue Robespierre
Beaurains 62217 FR
Other 510(k) Applications for this Company
Contact
Fadwa Bahr
Other 510(k) Applications for this Contact
Regulation Number
More FDA Info for this Regulation Number
Classification Product Code
OVD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/22/2020
Decision Date
04/01/2021
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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