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FDA 510(k)

NEUROSURICAL RETRACTORS - VARIOUS TYPES

K-Number: K892543 · 1989-05-05

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

Device Summary

NEUROSURICAL RETRACTORS - VARIOUS TYPES 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 K892543. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROSURICAL RETRACTORS - VARIOUS TYPES?

NEUROSURICAL RETRACTORS - VARIOUS TYPES 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 K892543.

When did NEUROSURICAL RETRACTORS - VARIOUS TYPES receive FDA 510(k) clearance?

NEUROSURICAL RETRACTORS - VARIOUS TYPES received FDA 510(k) clearance on 1989-05-05, under 510(k) number K892543.

Who is the listed applicant for NEUROSURICAL RETRACTORS - VARIOUS TYPES?

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 NEUROSURICAL RETRACTORS - VARIOUS TYPES?

The FDA product code for NEUROSURICAL RETRACTORS - VARIOUS TYPES is GZT.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: GZT)

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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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