AXON MP-1 MICROPOSITIONER— 510(k) K990683

Substantially Equivalent

Axon Instruments, Inc.

FDA 510(k) clearance K990683 for AXON MP-1 MICROPOSITIONER, Substantially Equivalent on 1999-11-03. Applicant: Axon Instruments, Inc..

Clearance details

Applicant: Axon Instruments, Inc.
Product code: Code HAW
Advisory panel: Neurology
Date received: 1999-03-03
Decision date: 1999-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Foster City, CA, US

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Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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