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Results for “ORTHOPILOT”

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109 devices foundsorted by relevance

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  • Orthopilot Tha FS961R

    Aesculap, Inc.,FDA registration: United States
    None Registry: GUDID Class:I

  • Orthopilot NP998R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Orthopilot Tha FS941R

    Aesculap, Inc.,FDA registration: United States
    None Registry: GUDID Class:I

  • Orthopilot NP637R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Orthopilot NP169P

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Orthopilot NM743

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Orthopilot NP603P

    Aesculap, Inc.,FDA registration: United States
    None Registry: GUDID Class:I

  • Orthopilot NM769R

    Aesculap, Inc.,FDA registration: United States
    Withdrawn Registry: GUDID Class:I

  • Orthopilot Tha FS959R

    Aesculap, Inc.,FDA registration: United States
    None Registry: GUDID Class:I

  • Orthopilot NQ935P

    Aesculap, Inc.,FDA registration: United States
    None Registry: GUDID Class:I

  • Orthopilot

    Aesculap AG,Germany Group of variants
    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Orthopilot

    Kinamed, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Orthopilot 2 Total Hip Arthroplasty (Tha) Version 3.0

    Aesculap Implant Systems, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Orthopilot 2

    Aesculap, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aesculap Orthopilot Next Generation

    Aesculap Implant Systems, LLC,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Orthopilot Next Generation, Model FS101-FS106

    Aesculap Implant System, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Orthopilot Next Generation-Uka Software, Model FS210

    Aesculap Implant System, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Orthopilot Hto Module

    Aesculap, Inc.,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 61-80 of 109