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FDA 510(k)

EQUIVABONE

K-Number: K090310 · 2009-03-24

ApplicantEtex Corp.
Decision Date2009-03-24
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EQUIVABONE is the device name listed in this FDA 510(k) record. The listed applicant is Etex Corp.. It received FDA 510(k) clearance on 2009-03-24 under 510(k) number K090310. 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 EQUIVABONE?

EQUIVABONE is a medical device that received FDA 510(k) clearance on 2009-03-24. The listed applicant is Etex Corp.. The 510(k) number is K090310.

When did EQUIVABONE receive FDA 510(k) clearance?

EQUIVABONE received FDA 510(k) clearance on 2009-03-24, under 510(k) number K090310.

Who is the listed applicant for EQUIVABONE?

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

What is the FDA product code for EQUIVABONE?

The FDA product code for EQUIVABONE is MQV.

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Other records listing Etex Corp. 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.

K100883CARRIGENK101557GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGENK093447CARRIGENK091729ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONEK091607ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONEK090855EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE

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Related Devices (Code: MQV)

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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.

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