FDA 510(k)

AltiVate® Anatomic Pegged Glenoid with Markers

Número K: K203026 · 2020-12-23

Data da decisão2020-12-23

Código do produtoKWS

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

AltiVate® Anatomic Pegged Glenoid with Markers is the device name listed in this FDA 510(k) record. The listed applicant is Encore Medical L.P.. It received FDA 510(k) clearance on 2020-12-23 under 510(k) number K203026. The device is classified under product code KWS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the AltiVate® Anatomic Pegged Glenoid with Markers?

AltiVate® Anatomic Pegged Glenoid with Markers is a medical device that received FDA 510(k) clearance on 2020-12-23. The listed applicant is Encore Medical L.P.. The 510(k) number is K203026.

When did AltiVate® Anatomic Pegged Glenoid with Markers receive FDA 510(k) clearance?

AltiVate® Anatomic Pegged Glenoid with Markers received FDA 510(k) clearance on 2020-12-23, under 510(k) number K203026.

Who is the listed applicant for AltiVate® Anatomic Pegged Glenoid with Markers?

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

What is the FDA product code for AltiVate® Anatomic Pegged Glenoid with Markers?

The FDA product code for AltiVate® Anatomic Pegged Glenoid with Markers is KWS.

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Outros registros que listam Encore Medical L.P. como candidato(a)

K252567AltiVate Reverse® ADLC Glenosphere K252974EMPOWR Knee K251833EMPOWR Acetabular® Liner Extension K252141AltiVate Reverse® Glenoid K251776EMPOWR Revision Knee™ (EMPOWR Revision VVC+, e+ Tibial Insert)K251241EMPOWR Revision Knee™ (EMPOWR Revision Knee™ Symmetric TT Cones)

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Fonte oficial

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