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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K102785

TRIMED RADIOCARPAL FUSION SYSTEM · TriMed, Inc. · decided 2011-08-19 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Total Wrist Fusion PlatesRFP-STDTrimed, INC.HRS00842188101328
Total Wrist Fusion PlatesRFP-SHBTrimed, INC.HRS00842188101335
Total Wrist Fusion PlatesRFP-STRTrimed, INC.HRS00842188101342