FDA UDI In Commercial Distribution 🇺🇸 United States

INTREPED, Intraosseous Fusion Device

DI: 00850055649088 · Model: 01-11220 · Auxano Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTREPED, Intraosseous Fusion Device
Primary DI
00850055649088
Version / Model
01-11220
Catalog Number
01-11220
Company Name
Auxano Medical LLC
Labeler DUNS
119185571
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-13
Public Version
3
Public Version Date
2025-02-06
Public Version Status
Update
Public Device Record Key
9fa26df8-9658-406e-aa7f-f28b9bb5ad2b

Device Description

INTREPED 12x20 implant

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 Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Primary 00850055649088

Customer Contacts

Phone
4402622000

Premarket Submissions

Submission Number Supplement Number
K231649 000