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FDA 510(k)

NEUROSURGICAL DRILLS: STILLE, HUDSON

K-Number: K892531 · 1989-05-05

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-05-05
Product CodeHBG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROSURGICAL DRILLS: STILLE, HUDSON is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-05-05 under 510(k) number K892531. The device is classified under product code HBG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROSURGICAL DRILLS: STILLE, HUDSON?

NEUROSURGICAL DRILLS: STILLE, HUDSON is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K892531.

When did NEUROSURGICAL DRILLS: STILLE, HUDSON receive FDA 510(k) clearance?

NEUROSURGICAL DRILLS: STILLE, HUDSON received FDA 510(k) clearance on 1989-05-05, under 510(k) number K892531.

Who is the listed applicant for NEUROSURGICAL DRILLS: STILLE, HUDSON?

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

What is the FDA product code for NEUROSURGICAL DRILLS: STILLE, HUDSON?

The FDA product code for NEUROSURGICAL DRILLS: STILLE, HUDSON is HBG.

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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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