New to this company and trying to get my head around it, so (a) sorry if this is a dumb question and (b) thank you in advance to anyone who can set me straight ...
I understand that Remplir has been available for sale in Australia for a number of years, and that there are apparently over 100 orthopedic and plastic surgeons using it, why would Orthocell be required to conduct a study in rats to make its 510(k) submission in the US?
Also, does anyone know which predicate device(s) Orthocell will nominate in its 510(k) submission?
TIA.
Ann: Quarterly Activity Report & Appendix 4C, page-19
-
- There are more pages in this discussion • 9 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)
Add OCC (ASX) to my watchlist
 (20min delay)
|
|||||
|
Last
36.5¢ |
Change
-0.005(1.35%) |
Mkt cap ! $76.49M | |||
| Open | High | Low | Value | Volume |
| 37.0¢ | 38.0¢ | 36.5¢ | $44.20K | 119K |
Buyers (Bids)
| No. | Vol. | Price($) |
|---|---|---|
| 1 | 93553 | 36.5¢ |
Sellers (Offers)
| Price($) | Vol. | No. |
|---|---|---|
| 37.0¢ | 4500 | 1 |
View Market Depth
| Last trade - 16.10pm 16/08/2024 (20 minute delay) ? |
| OCC (ASX) Chart |