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FDA 510(k) Application Details - K241234
Device Classification Name
Fastener, Fixation, Nondegradable, Soft Tissue
More FDA Info for this Device
510(K) Number
K241234
Device Name
Fastener, Fixation, Nondegradable, Soft Tissue
Applicant
OTS Medical Ltd.
14 Weizmann Street, Floor 16
Tel Aviv 6423914 IL
Other 510(k) Applications for this Company
Contact
Assaf Dekel
Other 510(k) Applications for this Contact
Regulation Number
888.3040
More FDA Info for this Regulation Number
Classification Product Code
MBI
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
05/02/2024
Decision Date
01/23/2025
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
FDA Source Information for K241234
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