510(k) K890090
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