MICROPERFORATION INSTRUMENT— 510(k) K001507

Substantially Equivalent

Smith & Nephew, Inc.

FDA 510(k) clearance K001507 for MICROPERFORATION INSTRUMENT, Substantially Equivalent on 2000-06-14. Applicant: Smith & Nephew, Inc..

Clearance details

Applicant: Smith & Nephew, Inc.
Product code: Code LXH
Advisory panel: Orthopedic
Date received: 2000-05-15
Decision date: 2000-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mansfield, MA, US

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Adverse events under product code LXH

product code LXH

Death: 11
Injury: 2,218
Malfunction: 31,318
Total: 33,547

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.