FDA UDI In Commercial Distribution 🇺🇸 United States

DENALI® Spinal System

DI: 10888857011342 · Model: 101-90339 · K2M, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DENALI® Spinal System
Primary DI
10888857011342
Version / Model
101-90339
Catalog Number
101-90339
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-06
Public Version
1
Public Version Date
2021-04-14
Public Version Status
New
Public Device Record Key
128732ed-0071-4bcb-b24a-8d0c8682e0e1

Device Description

Rod Cutter, Telescoping Handles Size Ø6.0 mm

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44805 Orthopaedic implantable-device cutter

Identifiers

Type ID
Primary 10888857011342

Customer Contacts