510(k) K002334

MACROPORENS CRANILOC by Macropore Biosurgery, Inc. — Product Code GXR

K002334 is an FDA 510(k) premarket notification submitted by Macropore Biosurgery, Inc. for the device "MACROPORENS CRANILOC". The FDA issued a decision of Substantially Equivalent on May 2, 2001. The device falls under product code GXR (Cover, Burr Hole), a Class II device regulated under 21 CFR 882.5250. Macropore Biosurgery, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 2001
Date Received
August 1, 2000
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cover, Burr Hole
Device Class
Class II
Regulation Number
882.5250
Review Panel
NE
Submission Type