OSTEONICS COMBINATION SCREW RING/BLOCKER— 510(k) K990158

Substantially Equivalent

Osteonics Corp.

FDA 510(k) clearance K990158 for OSTEONICS COMBINATION SCREW RING/BLOCKER, Substantially Equivalent on 1999-02-01. Applicant: Osteonics Corp..

Clearance details

Applicant: Osteonics Corp.
Product code: Code MNI
Advisory panel: Orthopedic
Date received: 1999-01-19
Decision date: 1999-02-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Allendale, NJ, US

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Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.