FDA UDI In Commercial Distribution 🇺🇸 United States

BOWTI

DI: 10705034015644 · Model: 172802020 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BOWTI
Primary DI
10705034015644
Version / Model
172802020
Catalog Number
172802020
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2022-11-29
Public Version Status
Update
Public Device Record Key
a75e1b75-5e63-415e-a6e2-ba2027d3b627

Device Description

BOWTI ANTERIOR BUTTRESS STAPLE 20mm

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
No
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
KWQ APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 10705034015644

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K021039 000