Instrument imtrp/ExSm

Trade Name

Instrument

Generic Name

Bone-resection orthopaedic reamer, reusable

Model / Ref / Catalog

imtrp/ExSm, IMTRP-EXSM

Primary DI / UDI-DI

05060296236304

FDA Product Code

HTO

GMDN Term

Bone-resection orthopaedic reamer, reusable

Device Class

Class I

Regulation Number

888.4540

GUDID distribution status

Not in Commercial Distribution

Sterilization Method

Moist Heat or Steam Sterilization

• Jts Extendeable Implant

  Class II

  FDA 510(k) K092138 Active Cleared 22 Mar 2011

• Jts Extendible Distal Femoral Implant

  Class II

  FDA 510(k) K133152 Active Cleared 22 Jan 2014

• Patient Specific Distal Femoral Open recall

  Class II

  FDA 510(k) K140898 Active Cleared 20 Jan 2015

• Mets Modular Total Femur

  Class II

  FDA 510(k) K121055 Active Cleared 19 Sep 2012

• Mets Modular Proximal Femur

  Class II

  FDA 510(k) K121056 Active Cleared 20 Sep 2012

• Sculptor Robotic Guidance Arm (RGA)

  Class II

  FDA 510(k) K121765 Active Cleared 11 Jan 2013

See all devices from Stanmore Implants Worldwide Ltd →