FDA UDI In Commercial Distribution 🇺🇸 United States

TiLock

DI: M719GMCS70550 · 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
M719GMCS70550
Version / Model
1
Catalog Number
GMCS70-55
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-27
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
544ce0ae-3a0c-4ede-ba7f-9a9fa5b40277

Device Description

7.0mm x 55mm 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
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary M719GMCS70550

Customer Contacts

Phone
5123817070

Device Sizes

Type Value Unit Text
Outer Diameter 7.0 Millimeter
Length 55 Millimeter