FDA UDI In Commercial Distribution 🇺🇸 United States

YUKON OCT Spinal System

DI: 10888857397293 · Model: 7601-15214-G1 · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
YUKON OCT Spinal System
Primary DI
10888857397293
Version / Model
7601-15214-G1
Catalog Number
7601-15214-G1
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-15
Public Version
4
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
31d73ad9-0710-42f7-89c8-4bed2142a32a

Device Description

Occipital Screw, Size Ø5.25x14 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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

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 10888857397293

Customer Contacts

Device Sizes

Type Value Unit Text
Length 14 Millimeter
Outer Diameter 5.25 Millimeter