EXCIA— 510(k) K061699

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K061699 for EXCIA, Substantially Equivalent on 2006-08-18. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code LWJ
Advisory panel: Orthopedic
Date received: 2006-06-16
Decision date: 2006-08-18
Decision: Substantially Equivalent
Clearance type: Special
Location: Center Valley, PA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LWJ

product code LWJ

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.