IMPLANTABLE CLIP
K-Number: K100090 · 2010-02-02
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Device Summary
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
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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