FDA Lags on 510(k) Medical Device Approvals
The Food & Drug Administration falls far short of its own goals for clearing medical device 510(k) clearance applications, according to an exclusive report from MassDevice.com.
BOSTON--(BUSINESS WIRE)--According to MassDevice.com,
the online business journal of the medical device industry, medical
device approval times under the Food & Drug Administration's 510(k)
clearance process jumped 30 percent between 2005 and 2008. MassDevice's
exclusive investigation of 10 years of FDA data, Eye
on the FDA: H1 2009, shows that approval times for medical
devices increased nearly 2 percent — while the number of 510(k)
applications declined more than 19 percent — even as the FDA's budgets
and staff levels rose.
In fact, contrary to its own goal of
clearing 90 percent of 510(k) applications for medical devices in 90
days, Eye
on the FDA: H1 2009 demonstrates that decision times are
trending significantly longer. For example, the average decision time
for 510(k) approvals was 113 days in 2008, compared with 87 days in
2005, an increase of 30 percent in just three years.
"Medical
device manufacturers should reconsider all timelines associated with the
510(k) clearance process for medical technology," said MassDevice
Publisher Brian Johnson. "Taking into account a new, more stringent
approach on the part of the FDA's new leadership and a comprehensive
institutional examination of the 510(k) process that will likely result
in recommendations for change, the regulatory path for new devices is
likely to become longer, more costly and more onerous in the near
future."
Eye
on the FDA: H1 2009 examines other key trends and data on the
FDA's 510(k) approvals process. Here's a small sampling:
* Average decision times for 510(k) clearances
* Average
decision times by device classification
* 10-year history of
510(k) clearance decision times and device classifications
* A
list of all the companies and devices that received 510(k) approvals
during H1 2009
* The most active geographic regions for 510(k)
approvals, by device classification
* Hottest sectors and
device classifications
MassDevice's new report, Eye
on the FDA: H1 2009, provides important insight into the trends
shaping how most medical devices make it into the marketplace.
About MassDevice.com
MassDevice.com
(www.MassDevice.com)
is the online business journal of the medical devices industry. The
company provides daily coverage and in-depth analysis of the trends and
issues driving the sector.
