FDA UDI In Commercial Distribution 🇺🇸 United States

CASPIAN® Spinal System

DI: 10888857014121 · Model: 1101-04025F · K2M, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CASPIAN® Spinal System
Primary DI
10888857014121
Version / Model
1101-04025F
Catalog Number
1101-04025F
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
2023-09-19
Public Version Status
Update
Public Device Record Key
f37e1d1e-2451-4d59-a582-c6fd040e35e8

Device Description

MESA®Mini 90° Screw

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
MNI ORTHOSIS, SPINAL PEDICLE FIXATION
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

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

Identifiers

Type ID
Primary 10888857014121

Customer Contacts

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Outer Diameter 4 Millimeter