510(k) K892903

MITEK ANCHOR DRILL by Mitek Surgical Products, Inc. — Product Code HTW

K892903 is an FDA 510(k) premarket notification submitted by Mitek Surgical Products, Inc. for the device "MITEK ANCHOR DRILL". The FDA issued a decision of Substantially Equivalent on October 6, 1989. The device falls under product code HTW (Bit, Drill), a Class I device regulated under 21 CFR 888.4540. Mitek Surgical Products, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 1989
Date Received
April 20, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bit, Drill
Device Class
Class I
Regulation Number
888.4540
Review Panel
OR
Submission Type