Skip to content
Scan

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

Clearance record K093533

ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0 · Materialise NV · decided 2010-02-17 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Zimmer Patient Specific Instruments00-5970-000-03Materialise NVJWH MBHE314005970000030
Zimmer Patient Specific Instruments00-5970-000-10Materialise NVHSX JWHE314005970000100
Zimmer Patient Specific Instruments00-5970-000-03Materialise NVJWH MBHE31400597000003