FDA UDI In Commercial Distribution 🇺🇸 United States

ONVOY

DI: 00193982454562 · Model: 6235.0310 · GLOBUS MEDICAL, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ONVOY
Primary DI
00193982454562
Version / Model
6235.0310
Company Name
GLOBUS MEDICAL, INC.
Labeler DUNS
139105691
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-24
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
3c1a9de3-ba45-41c0-a611-37480b991065

Device Description

Abduction Alignment Guide - 45 Deg

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
MBL Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00193982454562

Premarket Submissions

Submission Number Supplement Number
K213842 000