Primary Device ID | 00811767025607 |
NIH Device Record Key | fb89483d-7b2c-4081-b4db-f838da04679e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FREEDOM PRIMARY PCK |
Version Model Number | LFPSLD00-ML |
Company DUNS | 792030103 |
Company Name | MAXX ORTHOPEDICS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811767025607 [Primary] |
JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2017-02-28 |
00811767025713 | FEMORAL PRIMARY PCK A, RIGHT |
00811767025706 | FEMORAL PRIMARY PCK A, LEFT |
00811767025690 | FEMORAL PRIMARY PCK H, RIGHT |
00811767025683 | FEMORAL PRIMARY PCK H, LEFT |
00811767025676 | FEMORAL PRIMARY PCK G, RIGHT |
00811767025669 | FEMORAL PRIMARY PCK G, LEFT |
00811767025652 | FEMORAL PRIMARY PCK F, RIGHT |
00811767025645 | FEMORAL PRIMARY PCK F, LEFT |
00811767025638 | FEMORAL PRIMARY PCK E, RIGHT |
00811767025621 | FEMORAL PRIMARY PCK E, LEFT |
00811767025614 | FEMORAL PRIMARY PCK D, RIGHT |
00811767025607 | FEMORAL PRIMARY PCK D, LEFT |
00811767025591 | FEMORAL PRIMARY PCK C, RIGHT |
00811767025584 | FEMORAL PRIMARY PCK C, LEFT |
00811767025577 | FEMORAL PRIMARY PCK B, RIGHT |
00811767025560 | FEMORAL PRIMARY PCK B, LEFT |