FDA UDI In Commercial Distribution 🇺🇸 United States

RIGIDLOOP

DI: 03760304680229 · Model: BTB Adjustable Cortical System - XL · S.B.M
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RIGIDLOOP
Primary DI
03760304680229
Version / Model
BTB Adjustable Cortical System - XL
Catalog Number
232486
Company Name
S.B.M
Labeler DUNS
772462123
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-18
Public Version
2
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
d2d562ad-60a3-4457-afc9-3599dd24139d

Device Description

The RIGIDLOOP device consists of an adjustable nonabsorbable braided loop and titanium button, preloaded with traction threads, designed to be used for ACL reconstruction. The implant is supplied sterile, ready to use.

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
45062 Tendon/ligament bone anchor, non-bioabsorbable

Identifiers

Type ID
Primary 03760304680229

Customer Contacts

Phone
574-404-8348

Premarket Submissions

Submission Number Supplement Number
K151004 000