FDA UDI In Commercial Distribution 🇺🇸 United States

LxHA™

DI: M711LXT261640000 · Model: LXT26164000 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LxHA™
Primary DI
M711LXT261640000
Version / Model
LXT26164000
Catalog Number
LXT26164000
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-31
Public Version
2
Public Version Date
2023-10-25
Public Version Status
Update
Public Device Record Key
3d7e88c4-10de-44a7-b620-d5470bf112f8

Device Description

HA PEEK, Ta

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Package M711LXT261640001
Primary M711LXT261640000

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K190684 000

Device Sizes

Type Value Unit Text
Width 26 Millimeter
Height 16 Millimeter
Length 40 Millimeter
Angle 0 degree