FDA 510(k)

Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement

N.º K: K260536 · 2026-05-15

Fecha de decisión2026-05-15

Código de productoKWL

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement is the device name listed in this FDA 510(k) record. The listed applicant is Depuy Ireland UC. It received FDA 510(k) clearance on 2026-05-15 under 510(k) number K260536. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement?

Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is Depuy Ireland UC. The 510(k) number is K260536.

When did Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement receive FDA 510(k) clearance?

Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement received FDA 510(k) clearance on 2026-05-15, under 510(k) number K260536.

Who is the listed applicant for Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement?

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

What is the FDA product code for Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement?

The FDA product code for Prostalac Hip System, SmartSet V+G Dual Antibiotic Bone Cement is KWL.

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Otros registros que enlistan a Depuy Ireland UC como solicitante

K260480VELYS™ Robotic-Assisted Solution K261458Sistema de Rodilla Total ATTUNE; Sistema de Rodilla de Cemento Libre ATTUNE K253624INHANCE™ Reverse Shoulder System K253551VELYS™ Hip Navigation K253197Sistema de Rodilla Total ATTUNE™; Manguito de Revisión Sleeve LPS™ de Adaptadores Femorales K251292RECLAIM Monobloc Revision Femoral Stem

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Fuente oficial

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