Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Porcine Mineral Collagen Composite Moldable

K-Number: K201859 · 2020-09-11

Decision Date2020-09-11
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Porcine Mineral Collagen Composite Moldable is a medical device manufactured by Collagen Matrix, Inc.. It received FDA 510(k) clearance on 2020-09-11 under approval number K201859. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Porcine Mineral Collagen Composite Moldable?

Porcine Mineral Collagen Composite Moldable is a medical device that received FDA 510(k) clearance on 2020-09-11. It is manufactured by Collagen Matrix, Inc.. The 510(k) number is K201859.

When was Porcine Mineral Collagen Composite Moldable approved by the FDA?

Porcine Mineral Collagen Composite Moldable received FDA 510(k) clearance on 2020-09-11, under approval number K201859.

What company makes Porcine Mineral Collagen Composite Moldable?

Porcine Mineral Collagen Composite Moldable is manufactured by Collagen Matrix, Inc..

What is the FDA product code for Porcine Mineral Collagen Composite Moldable?

The FDA product code for Porcine Mineral Collagen Composite Moldable is NPM.

Related Clinical Trials

Other Devices by Collagen Matrix, Inc.

View all 16 devices →

Related Devices (Code: NPM)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.