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FDA 510(k)

NONPOWERED NEUROSURGICAL INSTRUMENT

K-Number: K953173 · 1995-10-03

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1995-10-03
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NONPOWERED NEUROSURGICAL INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1995-10-03 under 510(k) number K953173. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NONPOWERED NEUROSURGICAL INSTRUMENT?

NONPOWERED NEUROSURGICAL INSTRUMENT is a medical device that received FDA 510(k) clearance on 1995-10-03. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K953173.

When did NONPOWERED NEUROSURGICAL INSTRUMENT receive FDA 510(k) clearance?

NONPOWERED NEUROSURGICAL INSTRUMENT received FDA 510(k) clearance on 1995-10-03, under 510(k) number K953173.

Who is the listed applicant for NONPOWERED NEUROSURGICAL INSTRUMENT?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NONPOWERED NEUROSURGICAL INSTRUMENT?

The FDA product code for NONPOWERED NEUROSURGICAL INSTRUMENT is GWG.

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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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