FDA UDI In Commercial Distribution 🇺🇸 United States

SCREW, CORTICAL

DI: 00887868040337 · Model: 8150-36-100 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SCREW, CORTICAL
Primary DI
00887868040337
Version / Model
8150-36-100
Catalog Number
815036100
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
d00e2681-197e-4492-bb79-2c698ff9540c

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
HWC Screw, fixation, bone

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 00887868040337

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K905048 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 3.5MM X 100MM