FDA UDI In Commercial Distribution 🇺🇸 United States

neoWave C

DI: 00818345028005 · Model: 20-CFX-3207 · Ht Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
neoWave C
Primary DI
00818345028005
Version / Model
20-CFX-3207
Catalog Number
N/A
Company Name
Ht Medical, LLC
Labeler DUNS
080386764
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-17
Public Version
1
Public Version Date
2023-11-27
Public Version Status
New
Public Device Record Key
f98b4e1f-5a32-4818-954f-95011455d21e

Device Description

neoWave C Cervical Cage, 13W x 12D x 7H, 14 deg

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00818345028005

Customer Contacts

Phone
888-594-8633

Premarket Submissions

Submission Number Supplement Number
K180401 000
K222988 000