FDA UDI In Commercial Distribution 🇺🇸 United States

Signature™ Comprehensive®

DI: 00887868554391 · Model: 20-8090-009-01 · Orthosoft Inc
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Signature™ Comprehensive®
Primary DI
00887868554391
Version / Model
20-8090-009-01
Catalog Number
20-8090-009-01
Company Name
Orthosoft Inc
Labeler DUNS
205670032
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-09
Public Version
1
Public Version Date
2024-02-19
Public Version Status
New
Public Device Record Key
8d7e1c34-d93b-4f04-b150-037a92471679

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWS PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
MBF PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
PHX shoulder prosthesis, reverse configuration
QHE Shoulder arthroplasty implantation system

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 00887868554391

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K232425 000