510(k) K162321
K162321 is an FDA 510(k) premarket notification submitted by Restore Surgical, LLC Dba Instratek for the device "EasyClip Xpress". The FDA issued a decision of Substantially Equivalent on Feb 10, 2017. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Restore Surgical, LLC Dba Instratek has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 10, 2017
- Date Received
- Aug 19, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3030
- Review Panel
- OR
- Submission Type
- 510(k)