DEVICE: Titan™ (10381780467557)
Device Identifier (DI) Information
Titan™
LNR-0960-191-6S
In Commercial Distribution
LNR-0960-191-6S
Ascension Orthopedics, Inc.
LNR-0960-191-6S
In Commercial Distribution
LNR-0960-191-6S
Ascension Orthopedics, Inc.
RSS HXL Liner Standard, +6S
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
48092 | Polyethylene reverse shoulder prosthesis cup |
A sterile component of a reverse shoulder prosthesis that consists of a polyethylene (PE) cup intended to be attached to a humeral stem prosthesis, or humeral body component, and to articulate with the reverse shoulder head.
|
Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
PHX | shoulder prosthesis, reverse configuration |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K190588 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Special Storage Condition, Specify: Do Not Use If Package Is Damaged |
Clinically Relevant Size
[?]Size Type Text |
---|
Device Size Text, specify: 6S |
Device Size Text, specify: 0.784 Inch |
Device Record Status
68d40144-00f3-4b1c-a16b-85b00464360c
January 25, 2023
2
January 09, 2020
January 25, 2023
2
January 09, 2020
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)654-2873
custsvcnj@integralife.com
custsvcnj@integralife.com