FDA UDI In Commercial Distribution 🇺🇸 United States

AMP II

DI: 00190376709215 · Model: 614-104 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AMP II
Primary DI
00190376709215
Version / Model
614-104
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-18
Public Version
1
Public Version Date
2026-02-26
Public Version Status
New
Public Device Record Key
4e48111b-8f6d-40ee-a94d-21bbda8bed93

Device Description

AMP II Inserter Sleeve, C/C Right

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
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
MAX Intervertebral fusion device with bone graft, lumbar
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 00190376709215

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242364 000