EM ENT Navigated Suctions— 510(k) K153555

Substantially Equivalent

Medtronic Navigation, Inc.

FDA 510(k) clearance K153555 for EM ENT Navigated Suctions, Substantially Equivalent on 2016-04-07. Applicant: Medtronic Navigation, Inc.. Device class: 2.

Clearance details

Applicant
Medtronic Navigation, Inc.
Product code
Code PGW
Device class
Class 2
Regulation
21 CFR 882.4560
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Louisville, CO, US
Download summary PDFView on FDA.gov ↗

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More clearances from Medtronic Navigation, Inc.

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Adverse events under product code PGW

product code PGW
Malfunction
1,199
Total
1,199

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 K153555

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 K153555.

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