510(k) K963015
K963015 is an FDA 510(k) premarket notification submitted by Biopsys Medical, Inc. for the device "SURGICAL STAPLE MARKER DEVICE (MODIFY)". The FDA issued a decision of Substantially Equivalent on October 7, 1996. The device falls under product code GDW (Staple, Implantable), a Class II device regulated under 21 CFR 878.4750. Biopsys Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 7, 1996
- Date Received
- July 25, 1996
- Clearance Type
- Traditional
- 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