510(k) K011500
K011500 is an FDA 510(k) premarket notification submitted by Mentor Corp. for the device "MENTOR CONTOUR PROFILE TISSUE EXPANDER". The FDA issued a decision of Substantially Equivalent on December 3, 2001. The device falls under product code LCJ (Tissue Expander And Accessories), a Class U device. Mentor Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 3, 2001
- Date Received
- May 16, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tissue Expander And Accessories
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type