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

Clearance record K102401

HEMI IMPLANT; MINI HEMI IMPLANT · Vilex, Inc. · decided 2011-07-20 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Cannulated 1st MPJ Hemi ImplantCHI-1CHVILEX LLCKWD00841731106131
Cannulated 1st MPJ Hemi ImplantCHI-4CHVILEX LLCKWD00841731106254
Cannulated 1st MPJ Hemi ImplantCHI-2THVILEX LLCKWD00841731106193
Cannulated 1st MPJ Hemi ImplantCHI-5CHVILEX LLCKWD00841731106292
Cannulated 1st MPJ Hemi ImplantCHI-1THVILEX LLCKWD00841731106155
Cannulated 1st MPJ Hemi ImplantCHI-3CHVILEX LLCKWD00841731106216
Cannulated 1st MPJ Hemi ImplantCHI-2CHVILEX LLCKWD00841731106179
Cannulated 1st MPJ Hemi ImplantCHI-4THVILEX LLCKWD00841731106278
Cannulated 1st MPJ Hemi ImplantCHI-5THVILEX LLCKWD00841731106315
Cannulated 1st MPJ Hemi ImplantCHI-3THVILEX LLCKWD00841731106230