FDA UDI In Commercial Distribution 🇺🇸 United States

WaveForm TO

DI: 10889981235307 · Model: WO1-928161 · SEASPINE ORTHOPEDICS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WaveForm TO
Primary DI
10889981235307
Version / Model
WO1-928161
Catalog Number
WO1-928161
Company Name
SEASPINE ORTHOPEDICS CORPORATION
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-04
Public Version
1
Public Version Date
2021-05-12
Public Version Status
New
Public Device Record Key
dfb1f9e2-45d0-441a-889b-25672231185a

Device Description

Interbody, 9mm x 28mm x 16mm, 10 Deg, 3D

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PHM Intervertebral fusion device with bone graft, thoracic
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 10889981235307

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201755 000