DEVICE: EXPEDIUM (10705034107639)
Device Identifier (DI) Information
EXPEDIUM
186142650
In Commercial Distribution
186142650
DEPUY SPINE, LLC
186142650
In Commercial Distribution
186142650
DEPUY SPINE, LLC
EXPEDIUM SPINE SYSTEM CABLE/WIRE SCREW 4.5 x 6.0 x 50mm
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? |
---|---|---|---|---|
61325 | Bone-screw internal spinal fixation system, non-sterile |
An assembly of non-sterile implantable devices intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. Otherwise known as a pedicle screw instrumentation system, it typically consists of a combination of anchors (e.g., bolts, hooks, pedicle screws or other types), interconnection mechanisms (incorporating nuts, screws, sleeves, or bolts), longitudinal members (e.g., plates, rods, plate/rod combinations), and/or transverse connectors. Non-sterile disposable devices associated with implantation may be included.
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Active | true |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
OSH | Pedicle screw spinal system, adolescent idiopathic scoliosis |
NKB | Orthosis, spinal pedicle fixation, for degenerative disc disease |
KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
MNH | Orthosis, spondylolisthesis spinal fixation |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K081252 | 000 |
K111136 | 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
06f935d4-cf04-4792-93db-36bf95daa3b9
September 09, 2019
3
September 24, 2015
September 09, 2019
3
September 24, 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
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)255-2500
xx@xx.xx
xx@xx.xx