FDA UDI In Commercial Distribution 🇺🇸 United States

DENALI® Spinal System

DI: 10888857269002 · Model: 111-55565 · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENALI® Spinal System
Primary DI
10888857269002
Version / Model
111-55565
Catalog Number
111-55565
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-10
Public Version
5
Public Version Date
2019-02-27
Public Version Status
Update
Public Device Record Key
96949863-bd4d-4bad-8d65-af505ba60b81

Device Description

Straight Rod, Size Ø5.5x65 mm CoCr

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MNH Orthosis, spondylolisthesis spinal fixation
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNI ORTHOSIS, SPINAL PEDICLE FIXATION

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10888857269002

Customer Contacts

Device Sizes

Type Value Unit Text
Length 65 Millimeter
Outer Diameter 5.5 Millimeter