510(k) K890090

DANEK IRRIGATING BURR (DIB) SET by Danek Medical, Inc. — Product Code GFF

K890090 is an FDA 510(k) premarket notification submitted by Danek Medical, Inc. for the device "DANEK IRRIGATING BURR (DIB) SET". The FDA issued a decision of Substantially Equivalent on January 24, 1989. The device falls under product code GFF (Bur, Surgical, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4820. Danek Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1989
Date Received
January 10, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bur, Surgical, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type