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FDA 510(k)

DSM Biomedical Dental Bone Graft

K-Number: K170245 · 2017-05-16

Decision Date2017-05-16
Product CodeNPM
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DSM Biomedical Dental Bone Graft is a medical device manufactured by Kensey Nash Corporation Dba Dsm Biomedical. It received FDA 510(k) clearance on 2017-05-16 under approval number K170245. 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 DSM Biomedical Dental Bone Graft?

DSM Biomedical Dental Bone Graft is a medical device that received FDA 510(k) clearance on 2017-05-16. It is manufactured by Kensey Nash Corporation Dba Dsm Biomedical. The 510(k) number is K170245.

When was DSM Biomedical Dental Bone Graft approved by the FDA?

DSM Biomedical Dental Bone Graft received FDA 510(k) clearance on 2017-05-16, under approval number K170245.

What company makes DSM Biomedical Dental Bone Graft?

DSM Biomedical Dental Bone Graft is manufactured by Kensey Nash Corporation Dba Dsm Biomedical.

What is the FDA product code for DSM Biomedical Dental Bone Graft?

The FDA product code for DSM Biomedical Dental Bone Graft is NPM.

Related Clinical Trials

Other Devices by Kensey Nash Corporation Dba Dsm Biomedical

Related Devices (Code: NPM)

Official Source

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