FDA UDI In Commercial Distribution 🇺🇸 United States

TITAN™

DI: 10381780258704 · Model: GLN-0926-030-03A · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TITAN™
Primary DI
10381780258704
Version / Model
GLN-0926-030-03A
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-19
Public Version
5
Public Version Date
2023-01-25
Public Version Status
Update
Public Device Record Key
7379f211-f1bf-488e-9814-7a16821f13a9
Distribution End Date
2026-12-31

Device Description

The Fin-Lock Glenoid implant is part of the Titan Modular Shoulder System. It is an anchor peg that is used in patients with severely painful and/or disabled joint, fracture-dislocations, and other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable. The glenoid component is intended for cemented use only.

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED

GMDN Terms

Code Name
36259 Shoulder glenoid fossa prosthesis, prefabricated

Identifiers

Type ID
Secondary M269GLN092603003A1
Primary 10381780258704

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152047 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Large