AccessGUDID - DEVICE: MOJAVE Expandable Interbody System (10888857383128)

GUDID

Device Identifier (DI) Information

Brand Name: MOJAVE Expandable Interbody System
Version or Model: 7012-2132407C-G3
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 7012-2132407C-G3
Company Name: K2M, INC.

Primary DI Number: 10888857383128
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 146060863 *Terms of Use

Device Description: Expandable Interbody with Set Screw, Size 13x24x7-10 mm

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:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
34170	Vertebral body prosthesis	An implantable device designed to replace one or more vertebral body(s) that has collapsed or been surgically removed due to trauma, tumour or degenerative disease. Also known as a corpectomy or vertebrectomy spacer, it is in the form of a one-piece or modular hollow cylinder made of inorganic materials (e.g., metal, polymer). It is typically used with supplemental spinal fixation and/or bone graft, and some types are adjustable for in situ adjustment of prosthesis height to allow intraoperative distraction of adjacent vertebrae.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
MAX	Intervertebral fusion device with bone graft, lumbar

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

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

[?]

Size Type Text
Width: 13 Millimeter
Device Size Text, specify: 7-10 mm
Device Size Text, specify: Convex
Length: 24 Millimeter
Height: 7 Millimeter

Device Record Status

Public Device Record Key: 054b0e3b-4078-48a3-98a1-305d6b0e3f3a
Public Version Date: September 20, 2023
Public Version Number: 5
DI Record Publish Date: December 18, 2017