FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: 00190376397016 · Model: 320-11183000 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
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Primary DI
00190376397016
Version / Model
320-11183000
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-22
Public Version
2
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
52af8bb9-810b-4b11-b21e-df2ab80d73e2

Device Description

PSX Lordotic Expandable, 11 x 18 x 30mm, 20°

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00190376397016

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K211873 000

Device Sizes

Type Value Unit Text
Angle 20 degree
Height 11 Millimeter
Width 18 Millimeter
Length 30 Millimeter