FDA UDI In Commercial Distribution 🇺🇸 United States

SureLock™

DI: M543CM9614F1 · Model: CM-9614F · CAYENNE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SureLock™
Primary DI
M543CM9614F1
Version / Model
CM-9614F
Company Name
CAYENNE MEDICAL, INC.
Labeler DUNS
606719685
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-04
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
e963c387-1f37-4e0d-86e9-26820e5f82fe

Device Description

SureLock™ All-Suture Anchor, 1.4mm pre-loaded implant, Flexible Inserter

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBI Fastener, Fixation, Nondegradable, Soft Tissue

GMDN Terms

Code Name
46646 Orthopaedic bone screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary M543CM9614F1

Premarket Submissions

Submission Number Supplement Number
K132867 000