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FDA 510(k)

STATLOCK IV CONNECTOR AND ANCHOR SET

K-Number: K902109 · 1990-10-19

ApplicantVenetec, Inc.
Decision Date1990-10-19
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STATLOCK IV CONNECTOR AND ANCHOR SET is the device name listed in this FDA 510(k) record. The listed applicant is Venetec, Inc.. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K902109. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STATLOCK IV CONNECTOR AND ANCHOR SET?

STATLOCK IV CONNECTOR AND ANCHOR SET is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is Venetec, Inc.. The 510(k) number is K902109.

When did STATLOCK IV CONNECTOR AND ANCHOR SET receive FDA 510(k) clearance?

STATLOCK IV CONNECTOR AND ANCHOR SET received FDA 510(k) clearance on 1990-10-19, under 510(k) number K902109.

Who is the listed applicant for STATLOCK IV CONNECTOR AND ANCHOR SET?

The FDA 510(k) record lists Venetec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STATLOCK IV CONNECTOR AND ANCHOR SET?

The FDA product code for STATLOCK IV CONNECTOR AND ANCHOR SET is FPA.

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 Venetec, 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: FPA)

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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