DEVICE: G7® (00887868461224)

Device Identifier (DI) Information

G7®
010002655
In Commercial Distribution
010002655
Biomet Orthopedics, LLC
00887868461224
GS1

1
129278169 *Terms of Use
No description.
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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.
Active false
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FDA Product Code

[?]
Product Code Product Code Name
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
OQH Hip, semi-constrained, cemented, metal/polymer + additive, cemented
PBI prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive
LWZ TISSUE GRAFT OF LESS THAN 6MM
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
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FDA Premarket Submission

FDA Premarket Submission Number [?] Supplement Number [?]
K121874 000
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Sterilization

No
Yes
Sterilization Method [?]
Moist Heat or Steam Sterilization
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Storage and Handling

[?]
Storage and Handling
No storage/handling found
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Clinically Relevant Size

[?]
Size Type Text
Device Size Text, specify: 32 mm B
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Device Record Status

435f372d-7f38-4495-8929-71e8706d93c4
May 30, 2025
2
May 20, 2021
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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
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Secondary DI

[?]
Issuing Agency [?] Secondary DI Number
No Secondary DIs found
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Unit of Use DI

[?]
Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]
No
No
None
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Production Identifier(s) in UDI

[?]
Yes
No
No
No
No CLOSE

Customer Contact

[?]
+1(800)348-9500
customerservice@zimmerbiomet.com
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