FDA UDI In Commercial Distribution 🇺🇸 United States

IntraOp Alignment System

DI: 00190376601182 · Model: 505-410410 · ALPHATEC SPINE, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
IntraOp Alignment System
Primary DI
00190376601182
Version / Model
505-410410
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-01
Public Version
1
Public Version Date
2024-10-09
Public Version Status
New
Public Device Record Key
460d1cf1-dc5e-45e5-b5b2-e17fb65bbb4c

Device Description

IOA Tracking Markers 10 pack

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
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
No

Product Codes

Code Name
LLZ System, image processing, radiological
OWB Interventional fluoroscopic x-ray system
JAA System, x-ray, fluoroscopic, image-intensified

GMDN Terms

Code Name
46470 Orthopaedic/craniofacial implantation planning software

Identifiers

Type ID
Primary 00190376601182

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K240199 000