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510(k) Predicate Database
FDA 510(k) ClearanceLLZ

2D Hip Planning Software

FDA 510(k) K261352 · One Ortho

Clearance details

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510(k) number
K261352
Device name
2D Hip Planning Software
Applicant
One Ortho
Product code
LLZ
Decision
Substantially Equivalent
Decision date
Device class
Class 2
Regulation number
892.2050
Advisory committee
RA
Medical specialty
Radiology

Candidate predicate devices

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Other devices cleared under product code LLZ form a screening cohort, not a predicate determination. Compare intended use, technological characteristics, performance evidence, labeling, and current legal-marketing status before selecting a predicate.

Candidate predicate devices for K261352
510(k)DeviceApplicantDecision date
K263048Syngo Carbon Space (VA4)Siemens Healthineers AG
K261874Syneris PACS v.1.0.1.0Syneris
K262442HipStudio AnalysisReplasia BV
K261855Elucid PlaqueIQElucid Bioimaging, Inc.
K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.
K261861SPINEsim v1.0Mdsim S.A.
K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC
K261500KBA3D (v2.4.0)S.M.A.I.O
K262449AdvaViewADVAHEALTH SOLUTIONS, LLC
K261916NeuroQuant PETCortechs Labs, Inc.
K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)
K260588Cleerly LABSCleerly, Inc.
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Building a 510(k) around this device type?

Assyro turns predicate research into a substantial-equivalence comparison and an eSTAR-ready 510(k) workflow, so predicate strategy, testing evidence, and labeling stay aligned before FDA review.

  • PubMed
  • ClinicalTrials.gov
  • FDA
  • Health Canada
  • EMA
  • ICH
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