DEVICE: INSTRUMENT (07613327193305)
Device Identifier (DI) Information
INSTRUMENT
4845-2-963
In Commercial Distribution
4845-2-963
Howmedica Osteonics Corp.
4845-2-963
In Commercial Distribution
4845-2-963
Howmedica Osteonics Corp.
ANATO FEMORAL BROACH ALSO COMPATIBLE WITH ABG II
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? |
---|---|---|---|---|
36167 | Orthopaedic broach |
A surgical instrument that is designed as an elongated, tapered and serrated cutting tool intended for shaping and enlarging holes in bone tissue. This is a reusable device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
MEH | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate |
MBL | Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous |
LWJ | Prosthesis, hip, semi-constrained, metal/polymer, uncemented |
MAY | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish |
JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED |
KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented |
KWL | Prosthesis, hip, hemi-, femoral, metal |
HWC | Screw, fixation, bone |
LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
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: Side: LEFT |
Device Size Text, specify: Size: 3 |
Device Record Status
c7b4d1c6-4473-4362-b44d-b34746bec33e
November 25, 2022
4
September 24, 2016
November 25, 2022
4
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 |
---|---|
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