DEVICE: B-P TOTAL HIP SYSTEM (00814193024701)
Device Identifier (DI) Information
B-P TOTAL HIP SYSTEM
01-16-0815
Not in Commercial Distribution
01-16-0815
ENDOTEC, INC.
01-16-0815
Not in Commercial Distribution
01-16-0815
ENDOTEC, INC.
B-P MODULAR EXTENSION W/ULTRACOAT - 15 MM X 200 MM
Device Characteristics
Labeling does not contain MRI Safety Information | |
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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? |
---|---|---|---|---|
34162 | Bipolar humeral head outer component |
An implantable, hemisphere-shaped component of a bipolar partial shoulder prosthesis designed to interface with the glenoid fossa on its outer surface where it freely rotates, and interface with a humeral head prosthesis on its inner surface where it allows free rotation of the head. It is typically composed of an outer metal shell and an inner polyethylene (PE) liner.
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Active | true |
33695 | Bipolar femoral head outer component, hemiarthroplasty |
An implantable hemisphere-shaped device used as part of a partial hip replacement (femoral) and designed to interface with the acetabulum on its outer surface where it freely rotates, and interface with a femoral head prosthesis on its inner surface where it allows free rotation of the head. It is a one-piece device typically composed of an outer metal shell [e.g., cobalt-chrome (Co-Cr), titanium (Ti), stainless steel] and an inner polyethylene (PE) liner.
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Active | true |
33715 | Ceramic-on-polyethylene total hip prosthesis |
A sterile implantable artificial substitute for a diseased (e.g., arthritic) or injured hip joint consisting of matching femoral (head/shaft) and acetabular components articulated at a ceramic-on-polyethylene or cross-linked polyethylene (PE) interface. Fixation devices for implantation (e.g., screws and bolts) may be included and implantation may be performed with or without bone cement.
|
Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
JDI | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K905262 | 000 |
Sterilization
Storage and Handling
[?]Storage and Handling |
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Storage Environment Temperature: between 5 and 40 Degrees Celsius |
Handling Environment Temperature: between 5 and 40 Degrees Celsius |
Clinically Relevant Size
[?]Size Type Text |
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Length: 200 Millimeter |
Width: 15 Millimeter |
Device Record Status
dac89676-553b-4467-b4d4-7e7329e16dd9
April 10, 2024
7
September 17, 2015
April 10, 2024
7
September 17, 2015
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
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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