If you're interested in becoming a contributor or requesting changes then click here to join the discord
Difference between revisions of "Medtronic"
Landonodnal (talk | contribs) |
Landonodnal (talk | contribs) |
||
| (4 intermediate revisions by the same user not shown) | |||
| Line 25: | Line 25: | ||
*[[SenSight|SenSight]] | *[[SenSight|SenSight]] | ||
*[[Vanta|Vanta]] | *[[Vanta|Vanta]] | ||
| + | ==FDA== | ||
| + | Medtronic has 2809 medical devices registered with the FDA. Here are some of them: | ||
| + | {| class="wikitable" style="margin:auto" | ||
| + | |+ Examples of FDA Approved Devices ([[Medtronic_FDA_Devices | View List]]) | ||
| + | |- | ||
| + | ! Device ID !! Device Name !! Class !! Category !! PMA !! PMN | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P000058 P000058] || Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction || 3 || Orthopedic || True || False | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P020045 P020045] || Cardiac Ablation Percutaneous Catheter || 3 || Cardiovascular || True || False | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P890003 P890003] || Pulse Generator, Permanent, Implantable || 3 || Cardiovascular || True || False | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P930039 P930039] || Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes || 3 || Cardiovascular || True || False | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P000058 P000058] || Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction || 3 || Orthopedic || True || False | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K201100 K201100] || Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass || 2 || Cardiovascular || False || True | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K180122 K180122] || Mesh, Surgical, Polymeric || 2 || General, Plastic Surgery || False || True | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K182119 K182119] || Thoracolumbosacral Pedicle Screw System || 2 || Orthopedic || False || True | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K200074 K200074] || Interventional Fluoroscopic X-Ray System || 2 || Radiology || False || True | ||
| + | |- | ||
| + | | [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K171253 K171253] || Electrode, Pacemaker, Temporary || 2 || Cardiovascular || False || True | ||
| + | |} | ||
==Links== | ==Links== | ||
| + | |||
[https://www.medtronic.com/us-en/index.html Website] | [https://www.medtronic.com/us-en/index.html Website] | ||
[https://en.wikipedia.org/wiki/Medtronic Wikipedia] | [https://en.wikipedia.org/wiki/Medtronic Wikipedia] | ||
Latest revision as of 02:06, 18 April 2023
"Medtronic plc is an American-Irish registered medical device company that primarily operates in the United States. Neuromodulation is the second-oldest and third-largest department of Medtronic. Its products include neurostimulation systems and implantable drug delivery systems for chronic pain, common movement disorders, and urologic and gastrointestinal disorders. The department's revenues in 2014 amounted to $1.9 billion, or 11% of Medtronic's total revenues."
Founded in The United States around 1949, Medtronic produces noninvasive hardware and invasive hardware.
Medtronic makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.
BCI Categories: Open-Loop Efferent, Open-Loop Afferent
Neurosensing Technique(s): EEG
Neurostimulation Technique(s): DBS, PNS
Hardware
FDA
Medtronic has 2809 medical devices registered with the FDA. Here are some of them:
| Device ID | Device Name | Class | Category | PMA | PMN |
|---|---|---|---|---|---|
| P000058 | Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction | 3 | Orthopedic | True | False |
| P020045 | Cardiac Ablation Percutaneous Catheter | 3 | Cardiovascular | True | False |
| P890003 | Pulse Generator, Permanent, Implantable | 3 | Cardiovascular | True | False |
| P930039 | Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes | 3 | Cardiovascular | True | False |
| P000058 | Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction | 3 | Orthopedic | True | False |
| K201100 | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | 2 | Cardiovascular | False | True |
| K180122 | Mesh, Surgical, Polymeric | 2 | General, Plastic Surgery | False | True |
| K182119 | Thoracolumbosacral Pedicle Screw System | 2 | Orthopedic | False | True |
| K200074 | Interventional Fluoroscopic X-Ray System | 2 | Radiology | False | True |
| K171253 | Electrode, Pacemaker, Temporary | 2 | Cardiovascular | False | True |
Links
Website Wikipedia Crunchbase LinkedIn TwitterFacebook YouTube