FDA UDI In Commercial Distribution 🇺🇸 United States

Invictus

DI: 00190376431093 · Model: 55225-125-070 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Invictus
Primary DI
00190376431093
Version / Model
55225-125-070
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-20
Public Version
1
Public Version Date
2022-05-30
Public Version Status
New
Public Device Record Key
41e41b44-0f02-4ef9-abdf-23b13d10beb3

Device Description

Fenestrated Cannulated Extended Tab Polyaxial Reduction Screw Ø12.5mm X 70mm

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

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

Identifiers

Type ID
Primary 00190376431093

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K214006 000

Device Sizes

Type Value Unit Text
Length 70 Millimeter
Outer Diameter 12.5 Millimeter