510(k) K142519
K142519 is an FDA 510(k) premarket notification submitted by Implant Direct Sybron Manufacturing, LLC for the device "InterActive Complete Surgical Tray". The FDA issued a decision of Substantially Equivalent on April 15, 2015. The device falls under product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories), a Class II device regulated under 21 CFR 880.6850. Implant Direct Sybron Manufacturing, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 15, 2015
- Date Received
- September 8, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
- Device Class
- Class II
- Regulation Number
- 880.6850
- Review Panel
- HO
- Submission Type