FDA UDI In Commercial Distribution 🇺🇸 United States

TiLock

DI: M71930051300 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TiLock
Primary DI
M71930051300
Version / Model
1
Catalog Number
G300-5-130
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-29
Public Version
1
Public Version Date
2023-10-09
Public Version Status
New
Public Device Record Key
9edcda1c-2511-49a8-aa32-997602824c63

Device Description

130mm MIS Straight Rod

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary M71930051300

Customer Contacts

Phone
512-381-7070

Premarket Submissions

Submission Number Supplement Number
K100757 000

Device Sizes

Type Value Unit Text
Length 120 Millimeter