510(k) K250869

Device
Parietene™ Macroporous Mesh (PPM5050 )
Applicant
Sofradim Production
510(k) number
K250869
Product code
FTL
Decision
Substantially Equivalent (SESE)
Decision date
2025-04-23
Date received
2025-03-24
Regulation
878.3300
Classification name
Mesh, Surgical, Polymeric
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Jhony Mallet
Address
116 Ave. Du Formans Trévoux FR 01600 01600

FDA Registration Numbers

Source Documents

510(k) summary PDF

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