510(k) K082523
K082523 is an FDA 510(k) premarket notification submitted by Osstell AB for the device "OSSTELL ISQ IMPLANT STABILITY METER". The FDA issued a decision of Substantially Equivalent on September 26, 2008. The device falls under product code EKX (Handpiece, Direct Drive, Ac-Powered), a Class I device regulated under 21 CFR 872.4200. Osstell AB has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 26, 2008
- Date Received
- September 2, 2008
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Handpiece, Direct Drive, Ac-Powered
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type