DEVICE: INSTRUMENT (07613327208337)
Device Identifier (DI) Information
INSTRUMENT
1030-2246
In Commercial Distribution
1030-2246
Howmedica Osteonics Corp.
1030-2246
In Commercial Distribution
1030-2246
Howmedica Osteonics Corp.
TRIDENT ALL-POLY CUP TRIAL
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| No | |
| 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? |
|---|---|---|---|---|
| 58480 | Acetabulum prosthesis trial, prefabricated, reusable |
A copy of a final acetabular prosthesis designed to be used for trial reductions during hip arthroplasty to judge the correct size and position of the final acetabular prosthesis to be implanted. It is one of a set, or a set, of graduated sizes, is typically made of metal or polymer material and may be designed in the form of cages, shells, augments, or inserts. This is a reusable device intended to be sterilized prior to use.
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Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| MBL | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous |
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
| KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
| LWJ | Prosthesis, hip, semi-constrained, metal/polymer, uncemented |
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
| KWL | Prosthesis, hip, hemi-, femoral, metal |
| LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
| HWC | Screw, fixation, bone |
| MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
| MAY | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| Premarket Submission Number Not Available/Not Released | |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| No storage/handling found |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Lumen/Inner Diameter: 22.0 Millimeter |
| Outer Diameter: 46.0 Millimeter |
Device Record Status
a4d3da95-96c5-4dc6-9bae-63a8f3c1fb8d
December 21, 2020
5
September 24, 2016
December 21, 2020
5
September 24, 2016
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
[?]
No Customer Contact currently defined