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FDA 510(k)

OSTEOMIMETIC SYNTHETIC BONE MATRIX

K-Number: K051775 · 2005-09-06

ApplicantBiomimetic Pharmaceuticals, Inc.
Decision Date2005-09-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEOMIMETIC SYNTHETIC BONE MATRIX is the device name listed in this FDA 510(k) record. The listed applicant is Biomimetic Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2005-09-06 under 510(k) number K051775. 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 OSTEOMIMETIC SYNTHETIC BONE MATRIX?

OSTEOMIMETIC SYNTHETIC BONE MATRIX is a medical device that received FDA 510(k) clearance on 2005-09-06. The listed applicant is Biomimetic Pharmaceuticals, Inc.. The 510(k) number is K051775.

When did OSTEOMIMETIC SYNTHETIC BONE MATRIX receive FDA 510(k) clearance?

OSTEOMIMETIC SYNTHETIC BONE MATRIX received FDA 510(k) clearance on 2005-09-06, under 510(k) number K051775.

Who is the listed applicant for OSTEOMIMETIC SYNTHETIC BONE MATRIX?

The FDA 510(k) record lists Biomimetic Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSTEOMIMETIC SYNTHETIC BONE MATRIX?

The FDA product code for OSTEOMIMETIC SYNTHETIC BONE MATRIX is MQV.

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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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