RESORBABLE LACTOSORB-L ACL CROSSPIN— 510(k) K014305

Substantially Equivalent

Arthrotek, Inc.

FDA 510(k) clearance K014305 for RESORBABLE LACTOSORB-L ACL CROSSPIN, Substantially Equivalent on 2002-03-29. Applicant: Arthrotek, Inc..

Clearance details

Applicant: Arthrotek, Inc.
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 2001-12-31
Decision date: 2002-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.