FDA UDI In Commercial Distribution 🇺🇸 United States

KAESSMANN INTERLOCKING

DI: 00880304069008 · Model: CP250315 · Biomet Orthopedics, LLC
Product Codes
7
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KAESSMANN INTERLOCKING
Primary DI
00880304069008
Version / Model
CP250315
Catalog Number
CP250315
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-19
Public Version
4
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
6b80cc3c-ed10-4e75-b614-55085801a6f3

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate
MAY Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

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

Identifiers

Type ID
Primary 00880304069008

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100469 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5 MM 50 MM