Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K960539
Device Classification Name
Probe
More FDA Info for this Device
510(K) Number
K960539
Device Name
Probe
Applicant
KINETIKOS MEDICAL, INC.
3950 SORRENTO VALLEY BLVD.,
SAN DIEGO, CA 92121 US
Other 510(k) Applications for this Company
Contact
MARK G URBANSKI
Other 510(k) Applications for this Contact
Regulation Number
888.4540
More FDA Info for this Regulation Number
Classification Product Code
HXB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/07/1996
Decision Date
07/23/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact