FDA UDI Not in Commercial Distribution 🇺🇸 United States

Integra® Spider™ Limted Wrist Fusion System

DI: 10381780441373 · Model: SPIDERIMP · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Integra® Spider™ Limted Wrist Fusion System
Primary DI
10381780441373
Version / Model
SPIDERIMP
Catalog Number
SPIDERIMP
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-11
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
2d2bf70b-1a8a-41f3-bbd9-9a2bae18a5bd
Distribution End Date
2023-03-31

Device Description

SPIDER Implant Set

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRS Plate, fixation, bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Secondary M248SPIDERIMP1
Primary 10381780441373

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K991873 000