FDA UDI Not in Commercial Distribution 🇺🇸 United States

NeoFuse HA Enhanced PLIF/TLIF

DI: 00818345020177 · Model: A2410-09 · Ht Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NeoFuse HA Enhanced PLIF/TLIF
Primary DI
00818345020177
Version / Model
A2410-09
Company Name
Ht Medical, LLC
Labeler DUNS
080386764
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-07
Public Version
5
Public Version Date
2023-04-03
Public Version Status
Update
Public Device Record Key
7f56dc27-04cc-4c82-85f1-c4c331825949
Distribution End Date
2022-07-13

Device Description

HA CAGE 24L x 10W x 9H

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
Yes
Has Expiration Date
Yes
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
Primary 00818345020177

Customer Contacts

Phone
918-995-2090