FDA UDI Not in Commercial Distribution 🇺🇸 United States

BIO-ANCHOR

DI: 20845854030797 · Model: C6121H · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIO-ANCHOR
Primary DI
20845854030797
Version / Model
C6121H
Catalog Number
C6121H
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2019-03-21
Public Version Status
Update
Public Device Record Key
3bd0a433-df7b-4400-a9bb-f87e28a01260
Distribution End Date
2017-02-03

Device Description

3.5 X 10.5MM BIO-ANCHOR WITH DISPOSABLE DRIVER, PRELOADED 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
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
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
Primary 20845854030797

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K042778 000

Device Sizes

Type Value Unit Text
Length 10.5 Millimeter
Outer Diameter 3.5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY