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FDA 510(k)

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO

K-Number: K891203 · 1989-04-06

Decision Date1989-04-06
Product CodeLRW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO 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 1989-04-06 under 510(k) number K891203. The device is classified under product code LRW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS: THOREK, JORGENSEN, FINOCHIETTO?

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO is a medical device that received FDA 510(k) clearance on 1989-04-06. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891203.

When did SCISSORS: THOREK, JORGENSEN, FINOCHIETTO receive FDA 510(k) clearance?

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO received FDA 510(k) clearance on 1989-04-06, under 510(k) number K891203.

Who is the listed applicant for SCISSORS: THOREK, JORGENSEN, FINOCHIETTO?

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 SCISSORS: THOREK, JORGENSEN, FINOCHIETTO?

The FDA product code for SCISSORS: THOREK, JORGENSEN, FINOCHIETTO is LRW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Zinnanti Surgical Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 76 devices →

Related Devices (Code: LRW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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