FDA UDI In Commercial Distribution 🇺🇸 United States

TiLock Modular

DI: M719GMCS60600 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TiLock Modular
Primary DI
M719GMCS60600
Version / Model
1
Catalog Number
GMCS60-60
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-21
Public Version
1
Public Version Date
2023-07-31
Public Version Status
New
Public Device Record Key
bc5667a3-9533-488d-bb50-e17659b8f55d

Device Description

6.0mm X 60mm MODULAR CANNULATED SINGLE THREAD SCREW

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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
KWP Appliance, Fixation, Spinal Interlaminal
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

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

Identifiers

Type ID
Primary M719GMCS60600

Customer Contacts

Phone
512-381-7070

Premarket Submissions

Submission Number Supplement Number
K172469 000

Device Sizes

Type Value Unit Text
Width 6.0 Millimeter
Length 60 Millimeter