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FDA 510(k)

DB-Orthopedics

K-Number: K200752 · 2020-04-22

ApplicantDimensional Bioceramics, LLC
Decision Date2020-04-22
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DB-Orthopedics is the device name listed in this FDA 510(k) record. The listed applicant is Dimensional Bioceramics, LLC. It received FDA 510(k) clearance on 2020-04-22 under 510(k) number K200752. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DB-Orthopedics?

DB-Orthopedics is a medical device that received FDA 510(k) clearance on 2020-04-22. The listed applicant is Dimensional Bioceramics, LLC. The 510(k) number is K200752.

When did DB-Orthopedics receive FDA 510(k) clearance?

DB-Orthopedics received FDA 510(k) clearance on 2020-04-22, under 510(k) number K200752.

Who is the listed applicant for DB-Orthopedics?

The FDA 510(k) record lists Dimensional Bioceramics, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DB-Orthopedics?

The FDA product code for DB-Orthopedics is MQV.

Other records listing Dimensional Bioceramics, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K212353DB-EZ Bone Void FillerK210193DB-CompositeK182742DB-CMFK171161Dimensional Bioceramics Calcium Sulfate Device (DB-CSD)

Related Devices (Code: MQV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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