510(k) K904611
K904611 is an FDA 510(k) premarket notification submitted by Interpore Intl. for the device "INTERPORE CYLINDRICAL HEX IMPLANT". The FDA issued a decision of Substantially Equivalent on February 5, 1991. The device falls under product code DZE (Implant, Endosseous, Root-Form), a Class II device regulated under 21 CFR 872.3640. Interpore Intl. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 5, 1991
- Date Received
- October 11, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implant, Endosseous, Root-Form
- Device Class
- Class II
- Regulation Number
- 872.3640
- Review Panel
- DE
- Submission Type