DEVICE: INSTRUMENT (07613327214734)
Device Identifier (DI) Information
INSTRUMENT
2230-22F
In Commercial Distribution
2230-22F
Howmedica Osteonics Corp.
2230-22F
In Commercial Distribution
2230-22F
Howmedica Osteonics Corp.
TRIDENT CONSTRAINED INSERT TRIAL
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
No | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.
GMDN Preferred Term Name | GMDN Definition |
---|---|
Acetabulum trial prosthesis, 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 of trial hip prostheses that match the different anatomical structures of the hip joint. It 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. |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
KWL | Prosthesis, hip, hemi-, femoral, metal |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
MBL | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous |
MAY | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish |
HWC | Screw, fixation, bone |
KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
LWJ | Prosthesis, hip, semi-constrained, metal/polymer, uncemented |
LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
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 |
---|
Device Size Text, specify: Alpha Code: F |
Device Size Text, specify: Degree: 10.0 Degree |
Lumen/Inner Diameter: 22.0 Millimeter |
Device Record Status
11fee46a-c0c4-41d5-bcd5-78259e82b8ae
March 29, 2018
2
September 24, 2016
March 29, 2018
2
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 |
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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