Primary Device ID | 07630030884375 |
NIH Device Record Key | cdbfa683-7c04-4104-a96f-9ea186c19318 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M.U.S.T. Reduction Pedicle Screw |
Version Model Number | 03.50.757 |
Company DUNS | 488227125 |
Company Name | Medacta International SA |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07630030884375 [Primary] |
KWQ | Appliance, Fixation, Spinal Intervertebral Body |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-08-24 |
07630030884511 | Red. Cann. Ped. Scr. 4.5 x 50mm Sterile |
07630030884504 | Red. Cann. Ped. Scr. 4.5 x 45mm Sterile |
07630030884498 | Red. Cann. Ped. Scr. 4.5 x 40mm Sterile |
07630030884481 | Red. Cann. Ped. Scr. 4.5 x 35mm Sterile |
07630030884474 | Red. Cann. Ped. Scr. 4.5 x 30mm Sterile |
07630030884467 | Red. Cann. Ped. Scr. 4.5 x 25mm Sterile |
07630030884450 | Red. Cann. Ped. Scr. 4.5 x 20mm Sterile |
07630030884375 | Reduct. Ped. Scr. 4.0 x 50mm - Sterile |
07630030884368 | Reduct. Ped. Scr. 4.0 x 45mm - Sterile |
07630030884351 | Reduct. Ped. Scr. 4.0 x 40mm - Sterile |
07630030884344 | Reduct. Ped. Scr. 4.0 x 35mm - Sterile |
07630030884337 | Reduct. Ped. Scr. 4.0 x 30mm - Sterile |
07630030884320 | Reduct. Ped. Scr. 4.0 x 25mm - Sterile |
07630030884313 | Reduct. Ped. Scr. 4.0 x 20mm - Sterile |