FDA UDI In Commercial Distribution 🇺🇸 United States

Exceed™ Biplanar Expandable Interbody System

DI: 10840642171532 · Model: 10-7706 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Exceed™ Biplanar Expandable Interbody System
Primary DI
10840642171532
Version / Model
10-7706
Catalog Number
10-7706
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-06
Public Version
1
Public Version Date
2025-11-14
Public Version Status
New
Public Device Record Key
b241ab8d-342e-4f3c-b953-88012c0d68a4

Device Description

Push Rod Removal Tool

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 10840642171532

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K231275 000