FDA UDI In Commercial Distribution 🇺🇸 United States

Impulse Interbody Spacer System

DI: 00842048136231 · Model: 07-06T1426L08 · DEGEN MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Impulse Interbody Spacer System
Primary DI
00842048136231
Version / Model
07-06T1426L08
Catalog Number
07-06T1426L08
Company Name
DEGEN MEDICAL, INC.
Labeler DUNS
078812602
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-20
Public Version
1
Public Version Date
2021-12-28
Public Version Status
New
Public Device Record Key
99160379-fb40-4823-9108-200b22983496

Device Description

14H X 26L X 12W X 8DEG Impulse Lordotic Trial

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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00842048136231

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201287 000

Device Sizes

Type Value Unit Text
Angle 8 degree
Width 12 Millimeter
Height 14 Millimeter
Length 26 Millimeter