510(k) K220812
K220812 is an FDA 510(k) premarket notification submitted by MedShape, Inc. for the device "DynaClip® Bone Staple". The FDA issued a decision of Substantially Equivalent on August 19, 2022. The device falls under product code JDR (Staple, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. MedShape, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 19, 2022
- Date Received
- March 21, 2022
- 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