Optima Coil System— 510(k) K200030

Substantially Equivalent

Balt USA, LLC

FDA 510(k) clearance K200030 for Optima Coil System, Substantially Equivalent on 2020-02-01. Applicant: Balt USA, LLC. Device class: 2.

Clearance details

Applicant
Balt USA, LLC
Product code
Code HCG
Device class
Class 2
Regulation
21 CFR 882.5950
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Irvine, CA, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code HCG

product code HCG
Death
50
Injury
801
Malfunction
5,625
Total
6,476

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 K200030

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 K200030.

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