510(k) K060248
K060248 is an FDA 510(k) premarket notification submitted by Coapt Systems, Inc. for the device "ULTRATINE TRANSBLEPH". The FDA issued a decision of Substantially Equivalent on June 12, 2006. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Coapt Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 12, 2006
- Date Received
- January 31, 2006
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type