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ARIX System Bone Screw
Jeil Medical Corporation · Model 111-069-13 · UDI-DI 08800089446643
NDG
Prescription
1
510(k) clearances
7
Adverse events
1
Recalls
21
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-08-28 | Zimmer, Inc. | Zimmer recently conducted a review of historic packaging validations completed. Based on this review, it was determined that a subset of product packaged at a single Zimmer facili |
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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.