FDA 510(k)

Freedom Metaphyseal Cone Implants (Metaphyseal Cones)

Número K: K252777 · 2025-10-31

Data da decisão2025-10-31

Código do produtoMBH

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

Freedom Metaphyseal Cone Implants (Metaphyseal Cones) is the device name listed in this FDA 510(k) record. The listed applicant is Maxx Orthopedics, Inc.. It received FDA 510(k) clearance on 2025-10-31 under 510(k) number K252777. The device is classified under product code MBH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Freedom Metaphyseal Cone Implants (Metaphyseal Cones)?

Freedom Metaphyseal Cone Implants (Metaphyseal Cones) is a medical device that received FDA 510(k) clearance on 2025-10-31. The listed applicant is Maxx Orthopedics, Inc.. The 510(k) number is K252777.

When did Freedom Metaphyseal Cone Implants (Metaphyseal Cones) receive FDA 510(k) clearance?

Freedom Metaphyseal Cone Implants (Metaphyseal Cones) received FDA 510(k) clearance on 2025-10-31, under 510(k) number K252777.

Who is the listed applicant for Freedom Metaphyseal Cone Implants (Metaphyseal Cones)?

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

What is the FDA product code for Freedom Metaphyseal Cone Implants (Metaphyseal Cones)?

The FDA product code for Freedom Metaphyseal Cone Implants (Metaphyseal Cones) is MBH.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Outros registros que listam Maxx Orthopedics, Inc. como candidato(a)

K261563Freedom Total Knee System (E-Poly Tibial Liners)K261609Freedom Partial Knee System K253171Libertas Taper Short (TS) Uncemented Femoral Stem (Libertas TS Stem)K253314Freedom Infinia™ Total Knee System K253144Freedom® Total Knee System – Titan PCK Components K243634Maxx Libertas Bipolar Hip Head (Bipolar Hip)

Ver todos os 19 dispositivos →

Dispositivos Relacionados (Código: MBH)

K261275Unity Total Knee System, Unity Knee Cementless CR FemurCorin, Ltd.K261462LANDMARK Total Knee SystemSmith & Nephew, Inc.K253728EVOLUTION® AM BIOFOAM® Tibial SystemMicroport Orthopedics, Inc.K251840Zimmer® Persona® Personalized Knee SystemZimmer, Inc.K253189Persona the Personalized Knee System (Persona Porous Plasma Spray PPS Femurs)Zimmer, Inc.K253328GMK 3D Metal Tibial Tray ExtensionMedacta International S.A.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.