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FDA 510(k)

SAFETY SCREW CONNECTOR

K-Number: K113719 · 2012-04-20

ApplicantAbbott Laboratories
Decision Date2012-04-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SAFETY SCREW CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2012-04-20 under 510(k) number K113719. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY SCREW CONNECTOR?

SAFETY SCREW CONNECTOR is a medical device that received FDA 510(k) clearance on 2012-04-20. The listed applicant is Abbott Laboratories. The 510(k) number is K113719.

When did SAFETY SCREW CONNECTOR receive FDA 510(k) clearance?

SAFETY SCREW CONNECTOR received FDA 510(k) clearance on 2012-04-20, under 510(k) number K113719.

Who is the listed applicant for SAFETY SCREW CONNECTOR?

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

What is the FDA product code for SAFETY SCREW CONNECTOR?

The FDA product code for SAFETY SCREW CONNECTOR is KNT.

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Related Devices (Code: KNT)

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.

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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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