FDA UDI In Commercial Distribution 🇺🇸 United States

TENOLOK

DI: 10845854044674 · Model: T50S65 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TENOLOK
Primary DI
10845854044674
Version / Model
T50S65
Catalog Number
T50S65
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-27
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3f335660-8051-419e-b924-335c6ac71361

Device Description

T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guide Pin, and 6.5 mm Drill Bit

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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "Radiation Sterilization"]

Product Codes

Code Name
MBI Fastener, fixation, nondegradable, soft tissue

GMDN Terms

Code Name
44093 Arthroscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 10845854044674

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120841 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 7.0MM DRILL BIT
Device Size Text, specify 2.4MM GUIDE PIN
Device Size Text, specify 5.0 MM ANCHOR