510(k) K172561
K172561 is an FDA 510(k) premarket notification submitted by Changzhou Kangdi Medical Stapler Co., Ltd. for the device "Disposable Circular Stapler". The FDA issued a decision of Substantially Equivalent on Dec 5, 2017. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Changzhou Kangdi Medical Stapler Co., Ltd. has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 5, 2017
- Date Received
- Aug 25, 2017
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Staple, Implantable
- Device Class
- Class II
- Regulation Number
- 878.4750
- Review Panel
- SU
- Submission Type
- 510(k)