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Agree. FB is certainly going back down under $150. I'll buy more when it goes under $100. lol.
I agree. Just noticed the 10Q filing! Awesome! Go BETS!!!!
Thanks for the correction.
NO, it was not due today. 15 Calendar days puts the deadline on May 31st. NT 10Q was filed on May 16th.
Agreed! I loaded up as well! If ($3M) in revenue in 60 days is true, this will be in multi-pennies before launch. Go BETS!!
Note: Paddy Power is also an Irish Bookmaker. Over $800M in revenue.
Closely watching this trade in L2, it looks like some forces are cross trading themselves to take this down so they can load them up cheap. Go BETS! This should be in multiple pennies by August/September. Go BETS!!
Thanks to BETS for keeping up on its promise. Go BETS!!
BETS is doing the right thing by partnerships. Paddy Power is generating close to $800M in revenue. Go BETS!!
Awesome News!!
Online betting is a huge revenue generating business.
Paddy Power
Revenue: 881.6 million EUR (2014)
Net income: 144.9 million EUR (2014)
Tell me about it! I love it!!
I have started liking this company a lot!! Partnerships, sponsoring races, ABP with BHA, looks like a lot of good things coming this year for BETS.
This is GREAT NEWS! Kudos to management for understanding shareholder value and their plans for being honest and transparent. Go BETS!!!
Awesome! Thanks.
Yes, I checked them out and they are different. They really have done their DD to own 67M shares. That is a positive sign!!
Just got in with an entry level position here. I do like the prospects here after doing my DD. Is the 10Q expected by 4/15?
It is going up! Awaiting the big news should be easily over $5 next week!!
This could be over $4 by next week! Very tiny float and market cap. Go AMDA!! Holding strong.
Good news today. AMDA is really preparing for the huge launch. Way to go AMDA!! As predicted yesterday, uptrend has started. Still on REG SHO.
Yep..uptrend will begin from today. AMDA's new technology is far better than PEEK.
I think it is March 3rd.
Agree. Close to $5 minimum just with earnings and without the new product pipeline.
Agree. They are probably timing the Earnings and Good news to squeeze the shorts. FDA approval imminent.
I think this is normal profit taking and consolidation. Insiders have bought shares - filing out today!
Agree..first let this hold 15 cents. I think we should see a slow incline in price starting tomorrow.
Loading at these levels. Conversion has given me the opportunity to load up at these low prices! Before DEC 30th!!!
Go AMDA!!!
FDA Info on Amedica 510K
Device Classification Name intervertebral fusion device with bone graft, lumbar
510(k) Number K143518
Device Name Valeo Spacer System and Valeo II Interbody Fusion Device System
Applicant
Amedica Corp.
1885 west 2100 south
salt lake city, UT 84119
Applicant Contact william d. jordan
Correspondent
AMEDICA CORP.
1885 west 2100 south
salt lake city, UT 84118
Correspodent Contact william d jordan
Regulation Number 888.3080
Classification Product Code
MAX
Subsequent Product Code
ODP
Date Received 12/12/2014
Decision Date 10/02/2015
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K143518
Here is what is interesting. What does FDA mean by substantially equivalent SESE?
What is Substantial Equivalence
A 510(k) requires demonstration of substantial equivalence to another legally U.S. marketed device. Substantial equivalence means that the new device is at least as safe and effective as the predicate.
A device is substantially equivalent if, in comparison to a predicate it:
has the same intended use as the predicate; and
has the same technological characteristics as the predicate;
or
has the same intended use as the predicate; and
has different technological characteristics and the information submitted to FDA;
does not raise new questions of safety and effectiveness; and
demonstrates that the device is at least as safe and effective as the legally marketed device.
http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/HowtoMarketYourDevice/PremarketSubmissions/PremarketNotification510k/#se
FDA APPROVAL SOON!!
Insider selling?? Not looking good to me.
Here is the key wording from FDA on its Decision on Substantially Equivalent!!!
A device may not be marketed in the U.S. until the submitter receives a letter declaring the device substantially equivalent. If FDA determines that a device is not substantially equivalent, the applicant may:
resubmit another 510(k) with new data,
request a Class I or II designation through the de novo process
file a reclassification petition, or
submit a premarket approval application (PMA).
This is bargain at these levels. Bought more! DD is SOLID !!!
I am in for the ride!! Will buy whenever I have funds available. I am confident that FDA will APPROVE this as they have already given an Substantial Equivalence SESE Decision!!!
FDA Info on Amedica 510K
Device Classification Name intervertebral fusion device with bone graft, lumbar
510(k) Number K143518
Device Name Valeo Spacer System and Valeo II Interbody Fusion Device System
Applicant
Amedica Corp.
1885 west 2100 south
salt lake city, UT 84119
Applicant Contact william d. jordan
Correspondent
AMEDICA CORP.
1885 west 2100 south
salt lake city, UT 84118
Correspodent Contact william d jordan
Regulation Number 888.3080
Classification Product Code
MAX
Subsequent Product Code
ODP
Date Received 12/12/2014
Decision Date 10/02/2015
Decision substantially equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K143518
Here is what is interesting. What does FDA mean by substantially equivalent SESE?
What is Substantial Equivalence
A 510(k) requires demonstration of substantial equivalence to another legally U.S. marketed device. Substantial equivalence means that the new device is at least as safe and effective as the predicate.
A device is substantially equivalent if, in comparison to a predicate it:
has the same intended use as the predicate; and
has the same technological characteristics as the predicate;
or
has the same intended use as the predicate; and
has different technological characteristics and the information submitted to FDA;
does not raise new questions of safety and effectiveness; and
demonstrates that the device is at least as safe and effective as the legally marketed device.
http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/HowtoMarketYourDevice/PremarketSubmissions/PremarketNotification510k/#se
FDA APPROVAL SOON!!
Exactly! Typical P&D. Scamming novice traders into their trap. Pathetic!!
I never had a position just watching this from late yesterday. As predicted, this will go under .01 pretty soon. A very typical P&D. Anyone who took profits yesterday and today morning..good job!
Looks like a good P&D run..gap down tomorrow for sure.
Many more interesting things to come!!
I think the new symbol will be "GENI".
Welcome Genie Gateway! Good things ahead.