RESORB-X G— 510(k) K121606

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K121606 for RESORB-X G, Substantially Equivalent on 2013-01-17. Applicant: KLS-Martin L.P..

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code GWO
Advisory panel: Neurology
Date received: 2012-06-01
Decision date: 2013-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

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Adverse events under product code GWO

product code GWO

Malfunction: 583
Total: 583

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.