FDA UDI In Commercial Distribution 🇺🇸 United States

PROPEL

DI: 20845854014834 · Model: C8600 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
PROPEL
Primary DI
20845854014834
Version / Model
C8600
Catalog Number
C8600
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-05
Public Version
3
Public Version Date
2025-05-09
Public Version Status
Update
Public Device Record Key
94ba5b6d-c8b7-4731-a4f2-28a1145aaaca

Device Description

PROPEL CANNULATED INTERFERENCE SCREW, 9 MM X 20 MM

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 Conditional
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
HWC Screw, fixation, bone

GMDN Terms

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

Identifiers

Type ID
Package 30845854014831
Primary 20845854014834
Previous 10845854014837

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K874676 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY