FDA UDI In Commercial Distribution 🇺🇸 United States

Meridian

DI: 10889981285296 · Model: RA1-405530 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Meridian
Primary DI
10889981285296
Version / Model
RA1-405530
Catalog Number
RA1-405530
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-25
Public Version
3
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
f84fe613-58e6-4618-83c5-dd0b1493e6b2

Device Description

Fixed Angle Screw, 5.5mm Dia. x 30mm

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
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
KWQ Appliance, fixation, spinal intervertebral body
OVD Intervertebral fusion device with integrated fixation, lumbar
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 10889981285296

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K220711 000