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Zimmer Biomet Patient Specific Instruments
Materialise NV · Model KNM-ZB11-00-01 · UDI-DI 05420060310072
2
510(k) clearances
260
Adverse events
3
Recalls
36
Facilities
Description
ZB MRI PKA Guide and Bone Model kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
| 2015-08-31 | ConforMIS, Inc. | May contain small amounts of ethylene glycol residue |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.