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TRUE DAT BOSS...TIME FOR BEER #1
sorry bro 2.4 mill was all the free cash i had left
lmao possably
ok shot my wad for the day lol..someone elses turn
got some powder left gonna slap the ask hold on tight
I HAVE A 2,000,000 BID AT 0.0043 THEY ARE HIDEING IT TRYING TO BRING IT DOWN LMAO..WHY
cool link bro whats it supposed to show again ?
its a class 2 and its almost the same..thats how..thats what admd needs to prove that its the same or close to other class 2..follow
wtf are u talking about fella / chick..explain EXACTLY what ur trying to say???!!??!!!
DUDE WE GONNA GET APPROVED..thanks to that dude that linked that crap i found this approval..READ IT..
http://www.accessdata.fda.gov/cdrh_docs/reviews/DEN140030.pdf
what does that have to do with ADMD ?!? please explain cause I do not see our device there or anything like it
rofl what is this guys point??!!?? lol
remember that name SIRTEX...j/s
life changer
5,000,000 on the ask
with nothing on the bid
I agree u slap the ask and buy the rest of the groups shares
looks like we got serious sellers on the ask pushing it down
IT WAS 43.5
LOL WHATS THE 911 MEAN
there hideing my bid lol
idk but im buying again lol..let them sell
ok cool thx for that reply
Does anyone think that the device used to carry the y90 is what made the FDA kick back the first application >? because AMIC is useing the only dissolveable carrier and there is a concern about radiation leaks into the bone..where as other companys use gold or plat, etc..DISCUSS!!!
AGREE
Searching the FDA site the last few days it seems there is ALOT OF Yttrium-90 devices that have been APPROVED BY THE FDA!! (GOOD NEWS) so that being said means we have a GREAT chance of getting approval because our device IS equivlant to other devices on the market that have gotten approval
OK HERES ONE APPROVED ..LIKE AMIC'S !! THIS IS OFF THE FDA SITE
HomeMedical DevicesProducts and Medical ProceduresDevice Approvals and ClearancesRecently-Approved Devices
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2014 Device Approvals
SIR-Spheres®- P990065
This is a brief overview of information related to FDA's approval to market this product. See the links below to the Summary of Safety and Effectiveness and product labeling for more complete information on this product, its indications for use, and the basis for FDA's approval.
Product Name: SIR-Spheres®
Manufacturer: Sirtex Medical Inc.
Address: Centrecourt Business Park, Unit D4, 25-27 Paul Street North, P.O. Box 760, North Ryde, NSW, 1670, Australia
Approval Date: March 5, 2002
Approval Letter: http://www.accessdata.fda.gov/cdrh_docs/pdf/p990065a.pdf
What is it? SIR-Spheres® consists of tiny spheres of yttrium-90, a radioactive substance, that are injected into the liver to treat cancer.
How does it work? The physician injects the small spheres into the liver tumor through the common hepatic (liver) artery, or through the right or left hepatic artery. The spheres lodge in the area of the tumor, where the radiation helps slow the growth of the cancer cells. The radioactivity disappears within 11 days, but the spheres remain in the liver permanently. For a drawing of the whole digestive system go to: http://www.niddk.nih.gov/health/digest/pubs/digesyst/newdiges.htm
When is it used? SIR-Spheres ®is for the treatment of inoperable tumors from primary colorectal cancer that have spread to the liver.
What will it accomplish? For patients with advanced colorectal cancer that has spread to the liver, the addition of a single treatment of SIR-Spheres® , along with chemotherapy, acts to slow down the progress of the disease.
When should it not be used? SIR-Spheres ®should not be used in patients who:
have had previous external radiation therapy to the liver,
have fluid accumulations or have liver failure,
have markedly abnormal liver function test results,
have abnormal blood circulation resulting in abnormal return of blood from the liver to the stomach, pancreas or bowel,
have cancer that has spread to other areas of the body,
have been treated with the drug capecitabine within the two previous months,
will be treated with capecitabine at any time following treatment with SIR-Spheres , or
who have a blood clot in the portal vein.
Additional information: Summary of Safety and Effectiveness and labeling are available at: http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cftopic/pma/p
heres a slice from some research off of the FDA site about a similar device / product
This device was approved for marketing by the Therapeutic Goods Administration in Australia in
February 1998. This device is approved for unrestricted sale in Australia (within radiation safo;!ty
guidelines) and for export to nine other countries, these being Hong Kong, New Zealand, Philippines,
Thailand, South Korea, Taiwan, Japan, Singapore and Canada. There are no further regulatory
restrictions on the sale of the product in Hong Kong, Philippines, Thailand or New z~~aland, other
than radiation safety practices. SIR-Spheres® has not been withdrawn from marketing for any reason
relating to the safety or effectiveness of the device.
120 "FDA" days..means u wont hear anything till june
GOOD MORNING ADMD!!!!
thye could keep it quite for atlease 10 biz days..wich is 2 weeks
ok LOOK i told ya boy yesterday..chill with that kinda DD..keep it to your self..load up make more money
tomorrow is gonna be FUN FUN FUN...j/s
!!!!!!!
It would work like ..A company buys out B company for 500 million bucks..now u /by shares and get ur value
I agree
AGREE ///but dont be caught with ur pants down on that faithful day///FDA APPROVES ETC ETC
I gave my 3 month notice aswell
why this year son! like in months
Idk about that seems they were shorting IMO
EXACTLY..will be more that them looking to help...will be ALOT OF ELMO's