AccessGUDID - DEVICE: CAPRI™ Corpectomy Cage System (10888857371101)

GUDID

Device Identifier (DI) Information

Brand Name: CAPRI™ Corpectomy Cage System
Version or Model: 7512-21624L0-G3
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 7512-21624L0-G3
Company Name: K2M, INC.

Primary DI Number: 10888857371101
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 146060863 *Terms of Use

Device Description: Corpectomy Cage with Set Screw, Size 13x16mm, 20-24mm, 0°, 0-20°

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
PLR	Spinal vertebral body replacement device - Cervical
MQP	Spinal vertebral body replacement device

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K171704	000
K180665	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

[?]

Size Type Text
Length: 13 Millimeter
Width: 16 Millimeter
Height: 24 Millimeter
Device Size Text, specify: 0-20 Degrees
Device Size Text, specify: 20-24 mm

Device Record Status

Public Device Record Key: c14fab63-4def-4b39-a0bd-fe1af3060c23
Public Version Date: February 24, 2020
Public Version Number: 2
DI Record Publish Date: December 12, 2018