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FDA 510(k)

IMPLANTABLE CLIP

K-Number: K100090 · 2010-02-02

ApplicantGenicon
Decision Date2010-02-02
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IMPLANTABLE CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Genicon. It received FDA 510(k) clearance on 2010-02-02 under 510(k) number K100090. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTABLE CLIP?

IMPLANTABLE CLIP is a medical device that received FDA 510(k) clearance on 2010-02-02. The listed applicant is Genicon. The 510(k) number is K100090.

When did IMPLANTABLE CLIP receive FDA 510(k) clearance?

IMPLANTABLE CLIP received FDA 510(k) clearance on 2010-02-02, under 510(k) number K100090.

Who is the listed applicant for IMPLANTABLE CLIP?

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

What is the FDA product code for IMPLANTABLE CLIP?

The FDA product code for IMPLANTABLE CLIP is FZP.

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 Genicon 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: FZP)

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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