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FDA 510(k)

BONE ANCHOR SYSTEM III (BAS III)

K-Number: K990295 · 1999-03-05

ApplicantBoston Scientific Corp
Decision Date1999-03-05
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONE ANCHOR SYSTEM III (BAS III) is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1999-03-05 under 510(k) number K990295. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE ANCHOR SYSTEM III (BAS III)?

BONE ANCHOR SYSTEM III (BAS III) is a medical device that received FDA 510(k) clearance on 1999-03-05. The listed applicant is Boston Scientific Corp. The 510(k) number is K990295.

When did BONE ANCHOR SYSTEM III (BAS III) receive FDA 510(k) clearance?

BONE ANCHOR SYSTEM III (BAS III) received FDA 510(k) clearance on 1999-03-05, under 510(k) number K990295.

Who is the listed applicant for BONE ANCHOR SYSTEM III (BAS III)?

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

What is the FDA product code for BONE ANCHOR SYSTEM III (BAS III)?

The FDA product code for BONE ANCHOR SYSTEM III (BAS III) is MBI.

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Related Devices (Code: MBI)

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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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