FDA 510(k) Application Details - K242835

Device Classification Name	Suture, Surgical, Absorbable, Polydioxanone   More FDA Info for this Device
510(K) Number	K242835
Device Name	Suture, Surgical, Absorbable, Polydioxanone
Applicant	Suturion AB Scheeletorget 1 Lund 223 63 SE Other 510(k) Applications for this Company
Contact	Paan Hermansson Other 510(k) Applications for this Contact
Regulation Number	878.4840   More FDA Info for this Regulation Number
Classification Product Code	NEW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/19/2024
Decision Date	01/22/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review