FDA UDI In Commercial Distribution 🇺🇸 United States

DENALI® Spinal System

DI: 10888857268982 · Model: 111-55555 · K2M, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENALI® Spinal System
Primary DI
10888857268982
Version / Model
111-55555
Catalog Number
111-55555
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
21423306-6a62-4e96-be1c-8113ca5614e8

Device Description

Straight Rod, Size Ø5.5x55 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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 10888857268982

Customer Contacts

Device Sizes

Type Value Unit Text
Length 55 Millimeter
Outer Diameter 5.5 Millimeter