Primary Device ID | M572TPS000D00F021 |
NIH Device Record Key | e1677da2-75f3-4498-baf0-383f35883fa2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Identity Imprint PS Knee Replacement System |
Version Model Number | TPS-000-D00F1 |
Catalog Number | TPS-000-D00F |
Company DUNS | 808821883 |
Company Name | Conformis, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.com | |
Phone | 781-345-9001 |
customer-service@conformis.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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M572TPS000D00F021 [Primary] |
JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-04 |
Device Publish Date | 2024-06-26 |
M572TCR000D00F021 - Identity Imprint CR Knee Replacement System | 2024-07-04 CR FEMORAL INSTRUMENTS,ALL SIZES LEFT AND RIGHT |
M572TCR000D00T021 - Identity Imprint CR Knee Replacement System | 2024-07-04 CR TIBIAL INSTRUMENTS ALL SIZES LEFT OR RIGHT |
M572TPS000D00F021 - Identity Imprint PS Knee Replacement System | 2024-07-04PS Femoral INSTRUMENTS,ALL SIZES LEFT AND RIGHT |
M572TPS000D00F021 - Identity Imprint PS Knee Replacement System | 2024-07-04 PS Femoral INSTRUMENTS,ALL SIZES LEFT AND RIGHT |
M572TCR302T07S011 - Identity Imprint Porous CR | 2024-02-01 IDENTITY IMPRINT POROUS CR TIBIAL TRAY SIZE 7 |
00810933031817 - Calcar Planer Adapter Drop-in | 2023-12-13 Calcar Planer Adapter Drop-in ED-09733 |
M572POV0123208011 - Identity Imprint Porous CR | 2023-09-18 POROUS OVAL PATELLA, 32MM X 8MM, iPoly |
M572POV0123509011 - Identity Imprint Porous CR | 2023-09-18 POROUS OVAL PATELLA, 35MM X 9MM, iPoly |
M572POV0123809011 - Identity Imprint Porous CR | 2023-09-18 POROUS OVAL PATELLA, 38MM X 9MM, iPoly |