FDA UDI In Commercial Distribution 🇺🇸 United States

DENALI® MI Spinal System

DI: 10888857147751 · Model: M101-08590 · K2M, INC.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENALI® MI Spinal System
Primary DI
10888857147751
Version / Model
M101-08590
Catalog Number
M101-08590
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-05
Public Version
2
Public Version Date
2023-09-19
Public Version Status
Update
Public Device Record Key
a431120b-6ae0-4e65-807c-dd2671414448

Device Description

Cannulated Poly Screw, Size Ø8.5x90 mm

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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, fixation, spinal intervertebral body
OSH Pedicle screw spinal system, adolescent idiopathic scoliosis
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
NKB Thoracolumbosacral pedicle screw system
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 10888857147751

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 8.5 Millimeter
Length 90 Millimeter