FDA UDI In Commercial Distribution 🇺🇸 United States

Novel

DI: 00844856031333 · Model: 64893-013 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Novel
Primary DI
00844856031333
Version / Model
64893-013
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-02
Public Version
1
Public Version Date
2020-03-10
Public Version Status
New
Public Device Record Key
611018fa-ea2f-48ff-93fe-2d1fb26cf3fb

Device Description

SD Cage Trial, Small, 13 mm

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00844856031333

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080699 000

Device Sizes

Type Value Unit Text
Height 13 Millimeter
Length 22 Millimeter
Width 9 Millimeter