FDA UDI In Commercial Distribution 🇺🇸 United States

Solar™ Interbody Fusion System

DI: 00842048181880 · Model: 12-87S09 · DEGEN MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Solar™ Interbody Fusion System
Primary DI
00842048181880
Version / Model
12-87S09
Catalog Number
12-87S09
Company Name
DEGEN MEDICAL, INC.
Labeler DUNS
078812602
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-10
Public Version
1
Public Version Date
2024-06-18
Public Version Status
New
Public Device Record Key
24e5bb20-869d-40ca-9208-f70fcffc89b7

Device Description

Modular Distraction Wedge, 9mm

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
Yes
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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
56637 Orthopaedic surgical distractor, internal

Identifiers

Type ID
Primary 00842048181880

Customer Contacts