FDA UDI Not in Commercial Distribution 🇺🇸 United States

Alphatec Solus

DI: 00840967190402 · Model: 25960-114 · ALPHATEC SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Alphatec Solus
Primary DI
00840967190402
Version / Model
25960-114
Company Name
ALPHATEC SPINE, INC.
Labeler DUNS
602465783
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-02
Public Version
2
Public Version Date
2023-04-07
Public Version Status
Update
Public Device Record Key
2401b460-f637-423c-b31a-f6b7b9ec5746
Distribution End Date
2023-04-06

Device Description

SOLUS LUMBAR TRIAL, LARGE, 14mm, 7° LORDOTIC, BODY

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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00840967190402

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123993 000