FDA UDI Not in Commercial Distribution 🇺🇸 United States

Tenolok

DI: 20845854043780 · Model: T50S · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tenolok
Primary DI
20845854043780
Version / Model
T50S
Catalog Number
T50S
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-12
Public Version
2
Public Version Date
2021-02-11
Public Version Status
Update
Public Device Record Key
6b351705-e770-4470-be32-74d69d55e781
Distribution End Date
2021-02-11

Device Description

5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture

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

Product Codes

Code Name
MBI Fastener, fixation, nondegradable, soft tissue

GMDN Terms

Code Name
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 20845854043780

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120841 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.0 mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY