FDA UDI In Commercial Distribution 🇺🇸 United States

K2M General Instruments

DI: 10888857529601 · Model: PRO-1079-105 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
K2M General Instruments
Primary DI
10888857529601
Version / Model
PRO-1079-105
Catalog Number
PRO-1079-105
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-24
Public Version
1
Public Version Date
2022-04-01
Public Version Status
New
Public Device Record Key
cb94a3db-b0ce-40f7-80d9-501706fc06d0

Device Description

Lordotic Modular Trial Size 22x45x14 mm, 15°

Device Characteristics

Single Use
No
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
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 10888857529601

Customer Contacts

Device Sizes

Type Value Unit Text
Length 45 Millimeter
Width 22 Millimeter
Angle 15 degree
Height 14 Millimeter