510(k) K992656
K992656 is an FDA 510(k) premarket notification submitted by DePuy Orthopaedics, Inc. for the device "DEPUY TOTAL ELBOW SYSTEM". The FDA issued a decision of Substantially Equivalent on November 5, 1999. The device falls under product code JDC (Prosthesis, Elbow, Constrained, Cemented), a Class II device regulated under 21 CFR 888.3150. DePuy Orthopaedics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 5, 1999
- Date Received
- August 9, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Elbow, Constrained, Cemented
- Device Class
- Class II
- Regulation Number
- 888.3150
- Review Panel
- OR
- Submission Type