Zimmer Cas
Zimmer Cas holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2014, with 2 FDA device recalls on record.
Top product codes for Zimmer Cas
FDA recalls by Zimmer Cas
- Z-1701-2015 — Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
- Z-0495-2015 — PSI Knee System- Prosthesis, knee patellofemorotibial, semi-constrained, cemented, polymer/meal/polymer The Zimmer PSI Knee System is indicated as an orthopedic instrument system to assist in the positioning of knee replacement components.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Zimmer Cas
Data sourced from openFDA. This site is unofficial and independent of the FDA.