AccessGUDID - DEVICE: Morse Head (07613327016086)

GUDID

Device Identifier (DI) Information

Brand Name: Morse Head
Version or Model: 01-2200
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 01-2200
Company Name: Howmedica Osteonics Corp.

Primary DI Number: 07613327016086
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 058311945 *Terms of Use

Device Description: Femoral Head

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Metallic femoral head prosthesis	A sterile implantable artificial substitute for a diseased or injured femoral head that has an outer surface made of metal (e.g., titanium alloy). It is designed to be attached to the trunnion of a prosthetic femoral stem/shaft or a head/stem adaptor, and to articulate with an acetabulum prosthesis as part of a total hip arthroplasty (THA) or with a bipolar component as part of a partial hip arthroplasty. The device ranges in form from partially to fully spherical (ball-shaped) and is available in various sizes.

GMDN Preferred Term Name

GMDN Definition

Metallic femoral head prosthesis

A sterile implantable artificial substitute for a diseased or injured femoral head that has an outer surface made of metal (e.g., titanium alloy). It is designed to be attached to the trunnion of a prosthetic femoral stem/shaft or a head/stem adaptor, and to articulate with an acetabulum prosthesis as part of a total hip arthroplasty (THA) or with a bipolar component as part of a partial hip arthroplasty. The device ranges in form from partially to fully spherical (ball-shaped) and is available in various sizes.

FDA Product Code

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Product Code	Product Code Name
JDI	Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWY	Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented
LWJ	Prosthesis, hip, semi-constrained, metal/polymer, uncemented

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K910988	000
K993601	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

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Size Type Text
Device Size Text, specify: Offset: 0.0 Millimeter
Device Size Text, specify: Diameter: 22.0 Millimeter

Device Record Status

Public Device Record Key: 164c2b47-718e-4de3-b1e8-0d22b505e213
Public Version Date: July 06, 2018
Public Version Number: 3
DI Record Publish Date: September 24, 2015