FDA UDI In Commercial Distribution 🇺🇸 United States

Spider Limited Wrist Fusion System

DI: 00885556834671 · Model: 062808 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Spider Limited Wrist Fusion System
Primary DI
00885556834671
Version / Model
062808
Catalog Number
062808
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-19
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
bad4d8d5-1a97-4c63-8120-7233bb5ebab4

Device Description

SPIDER TITANIUM 2.8/8MM BONE SCREW

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
HRS Plate, fixation, bone

GMDN Terms

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

Identifiers

Type ID
Primary 00885556834671

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K991873 000