FDA UDI In Commercial Distribution 🇺🇸 United States

Illico

DI: 00844856043329 · Model: 73875-40 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Illico
Primary DI
00844856043329
Version / Model
73875-40
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
4
Public Version Date
2020-12-30
Public Version Status
Update
Public Device Record Key
8c247518-2799-4d5c-8929-8b4aaf1c2b6b

Device Description

Ti CANNULATED POLYAXIAL SCREW 7.5mm X 40mm

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
Yes
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
NKB Orthosis, spinal pedicle fixation, for degenerative disc disease

GMDN Terms

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

Identifiers

Type ID
Primary 00844856043329

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123623 000

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 7.5 Millimeter