SCISSORS: THOREK, JORGENSEN, FINOCHIETTO
K-Number: K891203 · 1989-04-06
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Device Summary
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.
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
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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