FDA 510(k)

VECTORVISION HIP AND HIP SR

K-Number: K072573 · 2007-10-11

Decision Date2007-10-11

Product CodeHAW

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

VECTORVISION HIP AND HIP SR is the device name listed in this FDA 510(k) record. The listed applicant is Brainlab AG. It received FDA 510(k) clearance on 2007-10-11 under 510(k) number K072573. 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 HIP AND HIP SR?

VECTORVISION HIP AND HIP SR is a medical device that received FDA 510(k) clearance on 2007-10-11. The listed applicant is Brainlab AG. The 510(k) number is K072573.

When did VECTORVISION HIP AND HIP SR receive FDA 510(k) clearance?

VECTORVISION HIP AND HIP SR received FDA 510(k) clearance on 2007-10-11, under 510(k) number K072573.

Who is the listed applicant for VECTORVISION HIP AND HIP SR?

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 HIP AND HIP SR?

The FDA product code for VECTORVISION HIP AND HIP SR 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.