510(k) K182461
K182461 is an FDA 510(k) premarket notification submitted by Tornier, Inc. for the device "LATITUDE EV Total Elbow Arthroplasty". The FDA issued a decision of Substantially Equivalent on December 27, 2018. The device falls under product code JDB (Prosthesis, Elbow, Semi-Constrained, Cemented), a Class II device regulated under 21 CFR 888.3160. Tornier, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 27, 2018
- Date Received
- September 10, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Elbow, Semi-Constrained, Cemented
- Device Class
- Class II
- Regulation Number
- 888.3160
- Review Panel
- OR
- Submission Type