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FDA 510(k)

OSTEOBOOST-BMA

K-Number: K062260 · 2006-10-26

ApplicantOrthos Limited
Decision Date2006-10-26
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OSTEOBOOST-BMA is the device name listed in this FDA 510(k) record. The listed applicant is Orthos Limited. It received FDA 510(k) clearance on 2006-10-26 under 510(k) number K062260. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEOBOOST-BMA?

OSTEOBOOST-BMA is a medical device that received FDA 510(k) clearance on 2006-10-26. The listed applicant is Orthos Limited. The 510(k) number is K062260.

When did OSTEOBOOST-BMA receive FDA 510(k) clearance?

OSTEOBOOST-BMA received FDA 510(k) clearance on 2006-10-26, under 510(k) number K062260.

Who is the listed applicant for OSTEOBOOST-BMA?

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

What is the FDA product code for OSTEOBOOST-BMA?

The FDA product code for OSTEOBOOST-BMA is FMF.

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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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