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FDA 510(k)

RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS

K-Number: K874630 · 1987-12-23

ApplicantDowns Surgical , Ltd.
Decision Date1987-12-23
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1987-12-23 under 510(k) number K874630. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS?

RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1987-12-23. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K874630.

When did RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS receive FDA 510(k) clearance?

RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS received FDA 510(k) clearance on 1987-12-23, under 510(k) number K874630.

Who is the listed applicant for RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS?

The FDA product code for RANGE OF TITANIUM NEUROSURGERY INSTRUMENTS is HAO.

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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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