FDA UDI In Commercial Distribution 🇺🇸 United States

Argo Knotless GENESYS

DI: 20653405988646 · Model: KBC55 · Conmed Corporation
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Argo Knotless GENESYS
Primary DI
20653405988646
Version / Model
KBC55
Catalog Number
KBC55
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-12
Public Version
2
Public Version Date
2024-08-14
Public Version Status
Update
Public Device Record Key
6be4d062-6107-4d90-bd67-937049c1cd0b

Device Description

5.5 mm Argo Knotless GENESYS Anchor

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
No

Product Codes

Code Name
MAI Fastener, fixation, biodegradable, soft tissue
MBI Fastener, fixation, nondegradable, soft tissue

GMDN Terms

Code Name
45061 Tendon/ligament bone anchor, bioabsorbable
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Package 30653405988643
Primary 20653405988646

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K240090 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius
Type
Storage Environment Temperature
Temperature Range
0 – 104 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE