FDA 510(k)

VECTORVISION CT-FREE KNEE

K-Number: K021306 · 2002-10-25

Decision Date2002-10-25

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VECTORVISION CT-FREE KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K021306. 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 CT-FREE KNEE?

VECTORVISION CT-FREE KNEE is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Brainlab AG. The 510(k) number is K021306.

When did VECTORVISION CT-FREE KNEE receive FDA 510(k) clearance?

VECTORVISION CT-FREE KNEE received FDA 510(k) clearance on 2002-10-25, under 510(k) number K021306.

Who is the listed applicant for VECTORVISION CT-FREE KNEE?

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 CT-FREE KNEE?

The FDA product code for VECTORVISION CT-FREE KNEE 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.