TRIGEN INTERTAN— 510(k) K040212

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K040212 for TRIGEN INTERTAN, Substantially Equivalent on 2004-02-20. Applicant: Smith & Nephew, Inc.. Device class: 2.

Clearance details

Applicant
Smith & Nephew, Inc.
Product code
Code JDS
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Memphis, TN, US
Download summary PDFView on FDA.gov ↗

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More clearances from Smith & Nephew, Inc.

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Adverse events under product code JDS

product code JDS
Injury
1,776
Malfunction
1,509
Total
3,285

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recalls naming K040212

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K040212.

Data sourced from openFDA. This site is unofficial and independent of the FDA.