FDA 510(k)

VECTORVISION OSTEOTOMY

K-Number: K042513 · 2005-02-10

Decision Date2005-02-10

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VECTORVISION OSTEOTOMY is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2005-02-10 under 510(k) number K042513. The device is classified under product code HAW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTORVISION OSTEOTOMY?

VECTORVISION OSTEOTOMY is a medical device that received FDA 510(k) clearance on 2005-02-10. The listed applicant is Brainlab AG. The 510(k) number is K042513.

When did VECTORVISION OSTEOTOMY receive FDA 510(k) clearance?

VECTORVISION OSTEOTOMY received FDA 510(k) clearance on 2005-02-10, under 510(k) number K042513.

Who is the listed applicant for VECTORVISION OSTEOTOMY?

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

What is the FDA product code for VECTORVISION OSTEOTOMY?

The FDA product code for VECTORVISION OSTEOTOMY is HAW.

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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.