Primary Device ID | M269PFP5010321 |
NIH Device Record Key | 4723c223-8c2f-4436-86d4-56be08758ae9 |
Commercial Distribution Discontinuation | 2023-03-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Construct® |
Version Model Number | PFP-5010-32 |
Catalog Number | PFP-5010-32 |
Company DUNS | 942377524 |
Company Name | Ascension Orthopedics, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com | |
Phone | +1(800)654-2873 |
custsvcnj@integralife.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10381780246602 [Primary] |
HIBCC | M269PFP5010321 [Secondary] |
HXI | PASSER, WIRE, ORTHOPEDIC |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
[M269PFP5010321]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-05-02 |
Device Publish Date | 2017-09-05 |
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