510(k) K243315

Device
ProGrip™ Self-Gripping Polypropylene Mesh
Applicant
Sofradim Production
510(k) number
K243315
Product code
FTL
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-17
Date received
2024-10-22
Regulation
878.3300
Classification name
Mesh, Surgical, Polymeric
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Nicolas Mickaël
Address
116 Ave. Du Formans Trévoux FR 01600 01600

FDA Registration Numbers

Source Documents

510(k) summary PDF

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