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FDA 510(k)

SKIN HOOKS, VARIOUS TYPES

K-Number: K891898 · 1989-04-12

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-04-12
Product CodeGDG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKIN HOOKS, 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 1989-04-12 under 510(k) number K891898. The device is classified under product code GDG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN HOOKS, VARIOUS TYPES?

SKIN HOOKS, VARIOUS TYPES 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 K891898.

When did SKIN HOOKS, VARIOUS TYPES receive FDA 510(k) clearance?

SKIN HOOKS, VARIOUS TYPES received FDA 510(k) clearance on 1989-04-12, under 510(k) number K891898.

Who is the listed applicant for SKIN HOOKS, 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 SKIN HOOKS, VARIOUS TYPES?

The FDA product code for SKIN HOOKS, VARIOUS TYPES is GDG.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: GDG)

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.

K900069MODIFIED PGL ABSORBABLE STAPLE*United States Surgical, A Division of Tyco HealthcK864425RAYLOR(TM) DISSECTING HOOKCedar Surgical, Inc.K843136BRIMFIELD CANNULATED GRASPING HOOKSBrimfield Scientific InstrumentsK841010SURGICAL HOOKS, VARIOUSPremier Dental Products Co.K812562SURGICAL RETRACTOR & ELASTIC STAYS, DISPHumboldt ProductsK791120MIDDLE EAR PICKS, HOOKS CURETTES,Xomed, Inc.

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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