FDA UDI Not in Commercial Distribution 🇺🇸 United States

YUKON OCT Spinal System

DI: 10888857412286 · Model: 7601-B40400 · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
YUKON OCT Spinal System
Primary DI
10888857412286
Version / Model
7601-B40400
Catalog Number
7601-B40400
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-29
Public Version
2
Public Version Date
2023-10-25
Public Version Status
Update
Public Device Record Key
0a01cd39-7202-4eca-a216-3f4950eb64d3
Distribution End Date
2023-10-24

Device Description

Straight Rod, Dual Hex Size Ø4.0x400 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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKG Orthosis, cervical pedicle screw spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 10888857412286

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K182182 000

Device Sizes

Type Value Unit Text
Length 400 Millimeter
Outer Diameter 4 Millimeter