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FDA 510(k)

BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER

K-Number: K070864 · 2007-06-01

ApplicantBiomet Osteobiologics
Decision Date2007-06-01
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Osteobiologics. It received FDA 510(k) clearance on 2007-06-01 under 510(k) number K070864. 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 BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER?

BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER is a medical device that received FDA 510(k) clearance on 2007-06-01. The listed applicant is Biomet Osteobiologics. The 510(k) number is K070864.

When did BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER receive FDA 510(k) clearance?

BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER received FDA 510(k) clearance on 2007-06-01, under 510(k) number K070864.

Who is the listed applicant for BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER?

The FDA 510(k) record lists Biomet Osteobiologics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER?

The FDA product code for BONEPLAST QS CALCIUM SULFATE BONE VOID FILLER 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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