FDA UDI In Commercial Distribution 🇺🇸 United States

Cadence™

DI: 10381780240198 · Model: 10203020 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Cadence™
Primary DI
10381780240198
Version / Model
10203020
Catalog Number
10203020
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-24
Public Version
8
Public Version Date
2023-02-21
Public Version Status
Update
Public Device Record Key
38a1c556-6e0b-4fec-bf9a-f083987ac512
Distribution End Date
2026-12-31

Device Description

Cadence Flex Shaft Drill is placed through the hole in the tibial trial to drill a post hole into the tibia for placement of the implant.

Device Characteristics

Single Use
No
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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
61235 Cannulated surgical drill bit, single-use

Identifiers

Type ID
Secondary M268102030201
Primary 10381780240198

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 2.56in Lx .282in diameter; 1.113in L x .186in diameter thread