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Contegra®
MEDTRONIC, INC. · Model 200H22 · UDI-DI 00643169357136
MWH
Prescription
0
510(k) clearances
1,133
Adverse events (50 deaths)
1
Recalls
1
Facilities
Description
CNDT 200H22 CONTEGRA GBR1 HDE TEMP IND
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-01-18 | Shelhigh, Inc. | Unapproved Device-Distribution of an unapproved device into interstate commerce. |
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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.