STRYKER SPINE AVS PL PEEK SPACER— 510(k) K050624

Substantially Equivalent

Stryker Spine

FDA 510(k) clearance K050624 for STRYKER SPINE AVS PL PEEK SPACER, Substantially Equivalent on 2005-04-11. Applicant: Stryker Spine.

Clearance details

Applicant: Stryker Spine
Product code: Code MQP
Advisory panel: Orthopedic
Date received: 2005-03-11
Decision date: 2005-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Allendale, NJ, US

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Adverse events under product code MQP

product code MQP

Injury: 372
Malfunction: 519
Total: 891

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.