DEVICE: uCentum™ comprehensive posterior system (04052536079698)
Device Identifier (DI) Information
uCentum™ comprehensive posterior system
CS 3804-085-055
In Commercial Distribution
CS 3804-085-055
Ulrich GmbH & Co. KG
CS 3804-085-055
In Commercial Distribution
CS 3804-085-055
Ulrich GmbH & Co. KG
Screw, pre-fixation, Ø 8.5 mm, length 55 mm perforated
Device Characteristics
MR Conditional | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.
GMDN Preferred Term Name | GMDN Definition |
---|---|
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. |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
MNH | Orthosis, spondylolisthesis spinal fixation |
MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
NKB | Orthosis, spinal pedicle fixation, for degenerative disc disease |
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 |
---|
No Device Sizes |
Device Record Status
0591df5b-668e-40ec-a8ca-967f972e853e
March 29, 2018
2
July 30, 2016
March 29, 2018
2
July 30, 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
[?]
+4907319654152
safety@ulrichmedical.com
safety@ulrichmedical.com