DEVICE: Pantheon System (08054752862616)
Device Identifier (DI) Information
Pantheon System
Shaft
In Commercial Distribution
0200992
ADLER ORTHO SPA
Shaft
In Commercial Distribution
0200992
ADLER ORTHO SPA
Pantheon Shaft L170mm
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? |
---|---|---|---|---|
61561 | Body femoral/tibial extension stem, uncoated |
A sterile implantable device intended to provide an extension of, or coupling with, other components of a modular femoral/tibial prosthesis in the medullary canal to compensate for bone loss during revision arthroplasty or bone resection. The device is a solid/dense body made of uncoated metal [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel]. Fixation devices for implantation (e.g., screws and bolts) may be included.
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Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented |
LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
MBL | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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Length: 170 Millimeter |
Device Record Status
9b8702af-e797-41c6-97a1-6652f5d726a3
March 10, 2025
1
February 28, 2025
March 10, 2025
1
February 28, 2025
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
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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