FDA UDI In Commercial Distribution 🇺🇸 United States

CASPIAN® Spinal System

DI: 10888857014367 · Model: 1101-04030ML · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPIAN® Spinal System
Primary DI
10888857014367
Version / Model
1101-04030ML
Catalog Number
1101-04030ML
Company Name
K2M, INC.
Labeler DUNS
146060863
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2023-09-14
Public Version Status
Update
Public Device Record Key
9cc5cd5b-1433-43f3-92a5-96ee23bbb02d

Device Description

DENALI®Mini Long Shank Screw Size Dia. 4.0x30 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 10888857014367

Customer Contacts

Device Sizes

Type Value Unit Text
Length 30 Millimeter
Outer Diameter 4 Millimeter