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

Clearance record K163044

ORTHOLOC® 3Di Ankle Fracture Plating System · Wrightmedicaltechnologyinc · decided 2017-01-26 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ORTHOLOC 3DI PLATING SYSTEM58889003WRIGHT MEDICAL TECHNOLOGY, INC.HRS00889797067225
ORTHOLOC 3DI PLATING SYSTEM58885130WRIGHT MEDICAL TECHNOLOGY, INC.HRS00889797067249
ORTHOLOC 3DI PLATING SYSTEM58889001WRIGHT MEDICAL TECHNOLOGY, INC.HRS00889797067218
ORTHOLOC 3DI PLATING SYSTEM58885110WRIGHT MEDICAL TECHNOLOGY, INC.HRS00889797067232