DEVICE: SureLOK MIS 3L (00840019936637)
Device Identifier (DI) Information
SureLOK MIS 3L
63-8700-CA-02
In Commercial Distribution
63-8700-CA-02
PRECISION SPINE, INC.
63-8700-CA-02
In Commercial Distribution
63-8700-CA-02
PRECISION SPINE, INC.
Implant Case 2 BOM (Side Load Rod)
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? |
|---|---|---|---|---|
| 67309 | Bone-screw internal spinal fixation system sterilization container/implant set |
A collection of non-sterile, implantable components of a bone-screw internal spinal fixation system (e.g., rods, screws, connectors, hooks) supplied within a reusable sterilization container (i.e., all under the same product code) to be sterilized before they are implanted as part of an internal spinal fixation procedure. The set provides the surgeon with a selection of implants (e.g., different sizes) during surgery, whereby unused implants maybe resterilised for subsequent implantation in another patient. This is a reusable device which includes single-use implants.
|
Active | true |
| 65116 | Bone-screw internal spinal fixation system rod |
An implantable component of a bone-screw internal spinal fixation system in the form of a thin cylinder intended to provide immobilization and stabilization of spinal segments in the treatment of various spinal instabilities or deformities, and also used as an adjunct to spinal fusion [e.g., for degenerative disc disease (DDD)]. This component is designed as a longitudinal (intervertebral) connecting element passing through the system’s implantable screw heads or hooks. It is available in various forms (e.g., straight, curved, rigid, flexible, with varying diameters); flexible types may allow small movements of the spine.
|
Active | true |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| MNH | Orthosis, Spondylolisthesis Spinal Fixation |
| MNI | Orthosis, Spinal Pedicle Fixation |
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
d5ca1de7-5a10-47bc-b3cd-7f1b875552c7
October 07, 2025
3
August 29, 2019
October 07, 2025
3
August 29, 2019
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