510(k) K070998

INION BIORESTORE by Inion OY — Product Code MQV

K070998 is an FDA 510(k) premarket notification submitted by Inion OY for the device "INION BIORESTORE". The FDA issued a decision of Substantially Equivalent on October 11, 2007. The device falls under product code MQV (Filler, Bone Void, Calcium Compound), a Class II device regulated under 21 CFR 888.3045. Inion OY has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 11, 2007
Date Received
April 9, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filler, Bone Void, Calcium Compound
Device Class
Class II
Regulation Number
888.3045
Review Panel
OR
Submission Type