DEVICE: G7® (00887868461897)

Device Identifier (DI) Information

G7®
010002727
In Commercial Distribution
010002727
Biomet Orthopedics, LLC
00887868461897
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?
32856 Orthopaedic implant impactor, reusable
A metal and/or plastic hand-held manual surgical instrument designed to position an orthopaedic implant within the body by transmission of an impact force that drives the implant into its final position. The proximal end of the instrument is a handle usually designed to absorb the impact from a surgical hammer or mallet, and the distal end is usually shaped to conform to the implant shape (flat or anatomically curved) or is shaped like a chisel handle to facilitate implant positioning. This is a reusable device.
Active false
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FDA Product Code

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

f706f818-bf35-47c8-a20b-fa1552ef5767
May 30, 2025
3
April 30, 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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