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

Clearance record K103111

FORZA SPACER SYSTEM · Orthofix, Inc. · decided 2011-03-23 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
FORZA87-1312Orthofix US LLCMAX18257200106158
FORZA87-1311Orthofix US LLCMAX18257200106141
FORZA87-1216Orthofix US LLCMAX18257200106103
FORZA87-1213Orthofix US LLCMAX18257200106073
FORZA87-1208Orthofix US LLCMAX18257200106028
FORZA89-0118Orthofix US LLCMAX18257200077038
FORZA89-0115Orthofix US LLCMAX18257200077007
FORZA89-0107Orthofix US LLCMAX18257200076925
FORZA89-0105Orthofix US LLCMAX18257200076901
FORZA89-0104Orthofix US LLCMAX18257200076895
FORZA89-0103Orthofix US LLCMAX18257200076888
FORZA87-1215Orthofix US LLCMAX18257200106097
FORZA87-1214Orthofix US LLCMAX18257200106080
FORZA87-1212Orthofix US LLCMAX18257200106066
FORZA87-1210Orthofix US LLCMAX18257200106042
FORZA87-1209Orthofix US LLCMAX18257200106035
FORZA89-0106Orthofix US LLCMAX18257200076918
FORZA89-0102Orthofix US LLCMAX18257200076871