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

Clearance record K111492

ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER MODEL 2.5, ZIMMER PATIENT SPECIFIC INSTRUMENTS · Materialise NV · decided 2011-10-13 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Zimmer Patient Specific Instruments00-5970-000-10Materialise NVHSX JWHE314005970000100