KLS-MARTIN MMF SCREW— 510(k) K980760

Substantially Equivalent

KLS-Martin L.P.

FDA 510(k) clearance K980760 for KLS-MARTIN MMF SCREW, Substantially Equivalent on 1999-12-21. Applicant: KLS-Martin L.P..

Clearance details

Applicant: KLS-Martin L.P.
Product code: Code DZL
Advisory panel: Dental
Date received: 1998-02-27
Decision date: 1999-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Port Riche, FL, US

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Adverse events under product code DZL

product code DZL

Injury: 168
Total: 168

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.