SPiN Thoracic Navigation System— 510(k) K170023

Substantially Equivalent

Veran Medical Technologies, Inc.

FDA 510(k) clearance K170023 for SPiN Thoracic Navigation System, Substantially Equivalent on 2017-05-15. Applicant: Veran Medical Technologies, Inc.. Device class: 2.

Clearance details

Applicant
Veran Medical Technologies, Inc.
Product code
Code JAK
Device class
Class 2
Regulation
21 CFR 892.1750
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
St. Louis, MO, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code JAK

product code JAK
Death
27
Injury
571
Malfunction
779
Total
1,377

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 K170023

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 K170023.

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