FDA UDI In Commercial Distribution 🇺🇸 United States

ENZA™-A Titanium ALIF

DI: B030EZAT303815150 · Model: EZAT-3038-1515 · CAMBER SPINE TECHNOLOGIES, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENZA™-A Titanium ALIF
Primary DI
B030EZAT303815150
Version / Model
EZAT-3038-1515
Company Name
CAMBER SPINE TECHNOLOGIES, LLC
Labeler DUNS
054205979
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-27
Public Version
3
Public Version Date
2020-02-05
Public Version Status
Update
Public Device Record Key
f0585910-9a8b-428e-8a77-b7a7c79226f9

Device Description

Bi-Convex 15° Lordotic, 30mm x 38mm, 15mm

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
57805 Metallic spinal fusion cage, non-sterile

Identifiers

Type ID
Primary B030EZAT303815150

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K153720 000
K173432 000

Device Sizes

Type Value Unit Text
Depth 30 Millimeter
Width 38 Millimeter
Height 15 Millimeter