Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K033252
Device Classification Name
Screw, Fixation, Bone
More FDA Info for this Device
510(K) Number
K033252
Device Name
Screw, Fixation, Bone
Applicant
Stryker Endoscopy
5900 OPTICAL CT.
SAN JOSE, CA 95138 US
Other 510(k) Applications for this Company
Contact
MELISSA MURPHY
Other 510(k) Applications for this Contact
Regulation Number
888.3040
More FDA Info for this Regulation Number
Classification Product Code
HWC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/08/2003
Decision Date
11/13/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OR - Orthopedic
Review Advisory Committee
OR - Orthopedic
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact