510(k) K032371
K032371 is an FDA 510(k) premarket notification submitted by Encore Medical L.P. for the device "TITANIUM MESH SYSTEM". The FDA issued a decision of Substantially Equivalent on Feb 12, 2004. The device falls under product code MQP (Spinal Vertebral Body Replacement Device), a Class II device regulated under 21 CFR 888.3060. Encore Medical L.P. has 81 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 12, 2004
- Date Received
- Aug 1, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Spinal Vertebral Body Replacement Device
- Device Class
- Class II
- Regulation Number
- 888.3060
- Review Panel
- OR
- Submission Type
- 510(k)