FDA UDI In Commercial Distribution 🇺🇸 United States

Proficient® Posterior Cervical Spine System

DI: 10840642127409 · Model: 21-8747 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Proficient® Posterior Cervical Spine System
Primary DI
10840642127409
Version / Model
21-8747
Catalog Number
21-8747
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ae76b003-604d-457d-a422-89c82c136aca

Device Description

Cannulated Extended-Tab Translational Screw, 5.0 mm × 24 mm

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
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10840642127409

Customer Contacts

Phone
203-944-9494