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Na 111860

by MAKO Surgical Corp.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

14 closed

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00848486002879 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Recalls

14 recalls · FDA

    • Terminated Z-1735-2022 FDA Class II initiated 8 Aug 2022

    Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.

    • Terminated Z-2745-2020 FDA Class II initiated 9 Jul 2020

    Characterization issue associated with the product. This issue may cause a discrepancy during bone preparation in certain Mako Total Hip procedures.

    • Terminated Z-2925-2018 FDA Class II initiated 24 Jul 2018

    Specific lots of the Vizadisc Knee Procedure Tracking Kit and Vizadisc Hip Procedure Tracking Kit have the potential to be damaged on the Vizadisc reflective material causing an inability to be detected by the camera.

    • Terminated Z-3182-2018 FDA Class II initiated 27 Dec 2017

    Communication-connection error.

    • Terminated Z-3131-2017 FDA Class II initiated 7 Aug 2017

    Software discrepancy of not showing all the EE constants, when the screen is filled.

    • Terminated Z-1411-2017 FDA Class II initiated 22 Dec 2016

    Five (5) AFMEA Risk Control Measures are missing from the MAKO RIO THA Application User Guides

    • Terminated Z-1193-2017 FDA Class II initiated 29 Sep 2016

    Failure of the Offset Cup Reamer Handle not engaging its mating components.

    • Terminated Z-1583-2016 FDA Class II initiated 23 Feb 2016

    Potential disassociation of the orientation pin.

    • Terminated Z-1588-2016 FDA Class II initiated 25 Nov 2015

    Stryker Orthpaedics became aware that there is the potential for the 210540 MAKOplasty Hip Array Kit Laminate 150230 to list two part numbers for the RIO Base Array, which is item #5 on the product table.

    • Terminated Z-0224-2016 FDA Class II initiated 16 Jul 2015

    The locking pin on the RIO Base Array is damaged during assembly onto the RIO Base Array Connector.

  • 3 recalls, same reason

    • Terminated Z-0829-2015 FDA Class II initiated 7 Oct 2014
    • Terminated Z-0830-2015 FDA Class II initiated 7 Oct 2014
    • Terminated Z-0828-2015 FDA Class II initiated 7 Oct 2014

    MAKO has identified the potential that the shell impactors may be damaged intraoperatively.

    • Terminated Z-1508-2016 FDA Class II initiated 30 Apr 2014

    Revision of the field manual

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Patient positioning sensor
Model / Ref / Catalog
111860
Primary DI / UDI-DI
00848486002879
FDA Product Code
OLO
GMDN Term
Patient positioning sensor
Device Class
Class II
Regulation Number
882.4560
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Patient positioning sensor

Cleared under the same submission (K121064)

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Cleared under the same submission (K141989)

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Cleared under the same submission (K170593)

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Other devices from MAKO Surgical Corp.

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No