FDA UDI In Commercial Distribution 🇺🇸 United States

Impulse AM Interbody Spacer System

DI: 00842048139331 · Model: 0722-1332L08 · DEGEN MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Impulse AM Interbody Spacer System
Primary DI
00842048139331
Version / Model
0722-1332L08
Catalog Number
0722-1332L08
Company Name
DEGEN MEDICAL, INC.
Labeler DUNS
078812602
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-21
Public Version
1
Public Version Date
2021-12-29
Public Version Status
New
Public Device Record Key
56ad679d-7815-46be-9653-f3f72ad0a753

Device Description

13H X 32L X 8W X 8DEG Impulse AM Lordotic Spacer

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
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 00842048139331

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K210090 000

Device Sizes

Type Value Unit Text
Width 8 Millimeter
Length 32 Millimeter
Angle 8 degree
Height 13 Millimeter