FDA 510(k)

OSSIOfiber™ Compression Screws

Número K: K193660 · 2020-07-30

Data da decisão2020-07-30

Código do produtoHWC

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

OSSIOfiber™ Compression Screws is the device name listed in this FDA 510(k) record. The listed applicant is OSSIO , Ltd.. It received FDA 510(k) clearance on 2020-07-30 under 510(k) number K193660. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the OSSIOfiber™ Compression Screws?

OSSIOfiber™ Compression Screws is a medical device that received FDA 510(k) clearance on 2020-07-30. The listed applicant is OSSIO , Ltd.. The 510(k) number is K193660.

When did OSSIOfiber™ Compression Screws receive FDA 510(k) clearance?

OSSIOfiber™ Compression Screws received FDA 510(k) clearance on 2020-07-30, under 510(k) number K193660.

Who is the listed applicant for OSSIOfiber™ Compression Screws?

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

What is the FDA product code for OSSIOfiber™ Compression Screws?

The FDA product code for OSSIOfiber™ Compression Screws is HWC. This falls under the Cardiovascular category.

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Outros registros que listam OSSIO , Ltd. como candidato(a)

K254077OSSIOfiber® Threaded Trimmable Fixation Nail K254055OSSIOfiber® Suture Anchor K252022OSSIOfiber® Interference Screw K251309OSSIOfiber® Suture Anchor K243760OSSIOfiber® Suture Anchor 2.5-3.5 mm K241932OSSIOfiber® Compression Staple

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Dispositivos Relacionados (Código: HWC)

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Fonte oficial

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