DEVICE: Versalock Periprosthetic Femur Plates System-GMReis (07899258612690)
Device Identifier (DI) Information
Versalock Periprosthetic Femur Plates System-GMReis
VA Cannulated Screw
In Commercial Distribution
327-51-20
GM DOS REIS INDUSTRIA E COMERCIO LTDA
VA Cannulated Screw
In Commercial Distribution
327-51-20
GM DOS REIS INDUSTRIA E COMERCIO LTDA
VERSALOCK VARIABLE ANGLE CANNULATED SCREW T25 Ø5.0x20.0mm Ti
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? |
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46647 | Orthopaedic fixation plate, non-bioabsorbable |
A non-bioabsorbable, non-customized, firm, implantable sheet intended to stabilize a fractured orthopaedic bone (excluding craniofacial and spinal) to treat a traumatic/pathological fracture, to fuse a joint (arthrodesis) and/or as part of an osteotomy. Typically attached to a bone of a limb, rib, sternum, or pelvis, it is designed to be fixed in place with screws; it does not incorporate a sleeve or blade. Instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be included with the plate.
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Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
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HRS | Plate, Fixation, Bone |
JDP | Condylar Plate Fixation Implant |
HWC | Screw, Fixation, Bone |
JDQ | Cerclage, Fixation |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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K201728 | 000 |
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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No Device Sizes |
Device Record Status
bcaea0a6-6a94-46b0-87b0-9930eb315628
January 22, 2024
1
January 12, 2024
January 22, 2024
1
January 12, 2024
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