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FDA 510(k)

CHISELS- FREER, LUCAS, ALEXANDER, BISHOP

K-Number: K891902 · 1989-04-12

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-04-12
Product CodeKGD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CHISELS- FREER, LUCAS, ALEXANDER, BISHOP 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 1989-04-12 under 510(k) number K891902. The device is classified under product code KGD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHISELS- FREER, LUCAS, ALEXANDER, BISHOP?

CHISELS- FREER, LUCAS, ALEXANDER, BISHOP is a medical device that received FDA 510(k) clearance on 1989-04-12. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891902.

When did CHISELS- FREER, LUCAS, ALEXANDER, BISHOP receive FDA 510(k) clearance?

CHISELS- FREER, LUCAS, ALEXANDER, BISHOP received FDA 510(k) clearance on 1989-04-12, under 510(k) number K891902.

Who is the listed applicant for CHISELS- FREER, LUCAS, ALEXANDER, BISHOP?

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 CHISELS- FREER, LUCAS, ALEXANDER, BISHOP?

The FDA product code for CHISELS- FREER, LUCAS, ALEXANDER, BISHOP is KGD.

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Related Devices (Code: KGD)

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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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