FDA UDI In Commercial Distribution 🇺🇸 United States

KASM

DI: 00822409007592 · Model: 669-2070 · Ortho Development Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KASM
Primary DI
00822409007592
Version / Model
669-2070
Company Name
Ortho Development Corporation
Labeler DUNS
876542390
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
4
Public Version Date
2019-09-23
Public Version Status
Update
Public Device Record Key
908ea25b-4914-4e99-972d-be6bc3485762

Device Description

Medium 45A/P x 70M/L Tibial Spacer Mold

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
Yes
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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER
MBB BONE CEMENT, ANTIBIOTIC

GMDN Terms

Code Name
45105 Orthopaedic cement spacer mould

Identifiers

Type ID
Primary 00822409007592

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K133449 000

Device Sizes

Type Value Unit Text
Width 70 Millimeter
Length 45 Millimeter