WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION)— 510(k) K963587

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K963587 for WRIGHT PLASTER OF PARIS BONE VOID FILLER KIT (SUBJECT TO REVISION), Substantially Equivalent on 1997-03-24. Applicant: Wrightmedicaltechnologyinc.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 1996-09-09
Decision date: 1997-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, 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.