Device
Single-use non-sterile implantable 5.5mm x 240mm rod-hex intended for posterior spinal fixation systems.
Manufacturer
TITAMED (PTY) LTD
TITAMED (PTY) LTD
Model: RH240
Catalog: RH240
DI: 06009699901135
Status: New
MRI: Labeling does not contain MRI Safety Information
Single-use: Yes
Rx: Yes
OTC: No
First Published: 2026-05-28
Current Version: 2026-06-05
Description
Single-use non-sterile implantable 5.5mm x 240mm rod-hex intended for posterior spinal fixation systems.
Sterilization
Method Types - Sterilization Method:
Moist Heat or Steam Sterilization
Device Sterile:
No
Sterilization Prior To Use:
Yes
Regulatory & Distribution
Record Status:
Published
Version Number:
1
Record Key:
f7d8f51d-c28b-42cd-9f95-7fb10316313c
Distribution Status:
In Commercial Distribution
DUNS Number:
635580744
Device Count:
1
DM Exempt:
No
Premarket Exempt:
No
HCT/P:
No
Kit:
No
Combination Product:
No
Lot/Batch Tracked:
Yes
Serial Number Tracked:
No
Manufacturing Date Tracked:
No
Expiration Date Tracked:
No
Donation ID Number Tracked:
No
Labeled Contains NRL:
No
Labeled No NRL:
No
Identifiers
Device ID:
06009699901135
Type:
Primary
Issuing Agency:
GS1
GMDN
Code: 65116
Name: Bone-screw internal spinal fixation system rod
Definition:
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.
FDA Product Codes
NKB
Thoracolumbosacral Pedicle Screw System
Premarket Submissions
Submission Number:
K070385
Supplement Number:
000