FDA UDI In Commercial Distribution 🇺🇸 United States

Proficient® Posterior Cervical Spine System

DI: 10840642177039 · Model: 11-8742 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Proficient® Posterior Cervical Spine System
Primary DI
10840642177039
Version / Model
11-8742
Catalog Number
11-8742
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-12
Public Version
1
Public Version Date
2026-01-20
Public Version Status
New
Public Device Record Key
18cada8a-67eb-4d92-9be0-662b9c3e8153

Device Description

Screw to Screw Connector, 35-46mm

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
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

Code Name
65114 Bone-screw internal spinal fixation system connector

Identifiers

Type ID
Primary 10840642177039

Customer Contacts

Phone
203-944-9494