Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K111536
Device Classification Name
Screw, Fixation, Bone
More FDA Info for this Device
510(K) Number
K111536
Device Name
Screw, Fixation, Bone
Applicant
METASURG
16350 PARK TEN PL., SUITE 101
HOUSTON, TX 77084 US
Other 510(k) Applications for this Company
Contact
JOSHUA SCOTT
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
06/02/2011
Decision Date
07/21/2011
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