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FDA 510(k)

Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments

N.º K: K253515 · 2026-08-24

SolicitanteBiomet Orthopedics, Inc.
Fecha de decisión2026-08-24
Código de productoJDI
Comité asesorOR
DecisiónSubstantially Equivalent

Resumen del dispositivo

Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Orthopedics, Inc.. It received FDA 510(k) clearance on 2026-08-24 under 510(k) number K253515. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments?

Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments is a medical device that received FDA 510(k) clearance on 2026-08-24. The listed applicant is Biomet Orthopedics, Inc.. The 510(k) number is K253515.

When did Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments receive FDA 510(k) clearance?

Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments received FDA 510(k) clearance on 2026-08-24, under 510(k) number K253515.

Who is the listed applicant for Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments?

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

What is the FDA product code for Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments?

The FDA product code for Zimmer Biomet OSS™ Orthopedic Salvage System OsseoTi® Sleeves and Augments is JDI.

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Dispositivos relacionados (Código: JDI)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K253434OSSTM Orthopedic Salvage SystemBiomet, Inc.K252824Evolve AP Cup, World Finned Cup, World G-Zero Liner and Oddball Femoral HeadSignature Orthopaedics Pty, Ltd.K243571Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained LinersZimmer BiometK240783Anthology Cuellos de Cadera; Cuellos de Cadera CPCS; Cabezas Femorales; Lineras de acetábulo R3; Cuellos de Cadera Spectron; Cuellos de Cadera SynergySmith & Nephew, Inc.K241716Global Modular Replacement System, Modular Replacement System, Modular Rotating Hinge Knee ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK240418Stryker Orthopaedics Hip Systems Labeling UpdateHowmedica Osteonics Corp., Dba Stryker Orthopaedics

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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