FDA UDI In Commercial Distribution 🇺🇸 United States

Novel

DI: 00844856013391 · Model: 64612-014 · ALPHATEC SPINE, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Novel
Primary DI
00844856013391
Version / Model
64612-014
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
5
Public Version Date
2020-12-31
Public Version Status
Update
Public Device Record Key
df0624ba-f7b0-4267-81bc-2288eceb1e10

Device Description

TL - PEEK SMALL SPACER - 22MMX10MMX14MM

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
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
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00844856013391

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080699 000

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Length 22 Millimeter
Height 14 Millimeter