COLLAGEN MATRIX ANORGANIC BONE MINERAL BONE GRAFT MATERIALS— 510(k) K062200

Substantially Equivalent

Collagen Matrix, Inc.

FDA 510(k) clearance K062200 for COLLAGEN MATRIX ANORGANIC BONE MINERAL BONE GRAFT MATERIALS, Substantially Equivalent on 2007-02-13. Applicant: Collagen Matrix, Inc..

Clearance details

Applicant: Collagen Matrix, Inc.
Product code: Code MQV
Advisory panel: Orthopedic
Date received: 2006-08-01
Decision date: 2007-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Franklin Lakes, NJ, 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.