Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K992474
Device Classification Name
Arthroscope
More FDA Info for this Device
510(K) Number
K992474
Device Name
Arthroscope
Applicant
MEDIFIX, INC.
8727 NARRAGANSETT
MORTON GROVE, IL 60053-0000 US
Other 510(k) Applications for this Company
Contact
GEORGE ALBUSECU
Other 510(k) Applications for this Contact
Regulation Number
888.1100
More FDA Info for this Regulation Number
Classification Product Code
HRX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
07/26/1999
Decision Date
09/23/1999
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact