FDA UDI In Commercial Distribution 🇺🇸 United States

Regatta® Plate

DI: 10889981319922 · Model: RP2-004003 · Seaspine Orthopedics Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Regatta® Plate
Primary DI
10889981319922
Version / Model
RP2-004003
Catalog Number
RP2-004003
Company Name
Seaspine Orthopedics Corporation
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-06
Public Version
3
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
5ba653c0-6ab3-48e7-b1d0-4b4645672d5c

Device Description

Plate Inserter Wrench

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
KQW Goniometer, nonpowered

GMDN Terms

Code Name
32871 Surgical torque wrench, reusable

Identifiers

Type ID
Primary 10889981319922

Premarket Submissions

Submission Number Supplement Number
K200885 000