FDA UDI In Commercial Distribution 🇺🇸 United States

AMP II

DI: 00190376706818 · Model: 616-1-10-S · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
AMP II
Primary DI
00190376706818
Version / Model
616-1-10-S
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
8511a4cb-e641-4f13-a58f-41759c1da9dd

Device Description

AMP II PLATE AND CENTER SCREW, 1-HOLE 10

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
No
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 00190376706818

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K242364 000

Device Sizes

Type Value Unit Text
Length 20 Millimeter
Width 11 Millimeter