FDA UDI In Commercial Distribution 🇺🇸 United States

Proficient® Posterior Cervical Spine System

DI: 10840642130171 · Model: 10-8114 · 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
10840642130171
Version / Model
10-8114
Catalog Number
10-8114
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-04
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
2e5a7669-b8c0-413b-838c-4a4265ca3e78

Device Description

Proficient® Tap, 5.5mm, NAV-M

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
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10840642130171

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K181596 000