PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE— 510(k) K990131

Substantially Equivalent

Interpore Cross Intl.

FDA 510(k) clearance K990131 for PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE, Substantially Equivalent on 1999-03-02. Applicant: Interpore Cross Intl..

Clearance details

Applicant: Interpore Cross Intl.
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 1999-01-14
Decision date: 1999-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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Adverse events under product code MQV

product code MQV

Death: 6
Injury: 435
Total: 441

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.