FDA UDI In Commercial Distribution 🇺🇸 United States

AMP-LTX

DI: 00190376601526 · Model: 622-2-202-S · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMP-LTX
Primary DI
00190376601526
Version / Model
622-2-202-S
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-09
Public Version
2
Public Version Date
2025-11-20
Public Version Status
Update
Public Device Record Key
5143c721-1b18-47ba-8862-c5b069466f3d

Device Description

AMP-LTX Plate, 2-Hole Offset Right with Center 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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00190376601526

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242147 000