FDA UDI In Commercial Distribution 🇺🇸 United States

Summit Patella Plating System

DI: 00860004838005 · Model: Standard · Endeavor Orthopaedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Summit Patella Plating System
Primary DI
00860004838005
Version / Model
Standard
Catalog Number
1316-3000
Company Name
Endeavor Orthopaedics, LLC
Labeler DUNS
107767417
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-03
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
ffd295f5-b905-4016-92b3-be3a1021cf0c

Device Description

Sterile, Single use, Patella Fracture Repair Kit, Standard

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRS Plate, Fixation, Bone
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

GMDN Terms

Code Name
61688 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, sterile

Identifiers

Type ID
Primary 00860004838005

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K203408 000