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FDA 510(k)

NEURO SECTOR FIXATION DEVICE

K-Number: K833522 · 1984-05-25

ApplicantAdvanced Technology Laboratories, Inc.
Decision Date1984-05-25
Product CodeGXW
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEURO SECTOR FIXATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Technology Laboratories, Inc.. It received FDA 510(k) clearance on 1984-05-25 under 510(k) number K833522. The device is classified under product code GXW. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURO SECTOR FIXATION DEVICE?

NEURO SECTOR FIXATION DEVICE is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Advanced Technology Laboratories, Inc.. The 510(k) number is K833522.

When did NEURO SECTOR FIXATION DEVICE receive FDA 510(k) clearance?

NEURO SECTOR FIXATION DEVICE received FDA 510(k) clearance on 1984-05-25, under 510(k) number K833522.

Who is the listed applicant for NEURO SECTOR FIXATION DEVICE?

The FDA 510(k) record lists Advanced Technology Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEURO SECTOR FIXATION DEVICE?

The FDA product code for NEURO SECTOR FIXATION DEVICE is GXW.

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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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