FDA UDI In Commercial Distribution 🇺🇸 United States

PONTiS Achilles Tendon Repair System

DI: 00859210006070 · Model: 600-4001 · PONTIS ORTHOPAEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PONTiS Achilles Tendon Repair System
Primary DI
00859210006070
Version / Model
600-4001
Catalog Number
600-4001
Company Name
PONTIS ORTHOPAEDICS, LLC
Labeler DUNS
047775061
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-01
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
93cd59fc-c656-45e8-9757-5007351a9220

Device Description

PONTiS Achilles Tendon Repair Implant kit with Multifilament Stainless Steel Sutures and SS Crimp. Each Kit contains: 1x size #3 MFSS suture with 2 curved needles (white wrap) 1x size #3 MFSS suture with 2 curved needles (black wrap) 1x SS Crimp Collar for #3 SS sutures Supplied pouched, sterilized with EO.

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
MR Unsafe
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
GAQ Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile

GMDN Terms

Code Name
13904 Metallic suture, multifilament

Identifiers

Type ID
Primary 00859210006070

Customer Contacts

Phone
415-567-8935

Device Sizes

Type Value Unit Text
Device Size Text, specify Size #3 Suture