510(k) K190817
K190817 is an FDA 510(k) premarket notification submitted by Riverpoint Medical for the device "HS Fiber". The FDA issued a decision of Substantially Equivalent on May 1, 2019. The device falls under product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene), a Class II device regulated under 21 CFR 878.5000. Riverpoint Medical has 38 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 1, 2019
- Date Received
- Apr 1, 2019
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Nonabsorbable, Synthetic, Polyethylene
- Device Class
- Class II
- Regulation Number
- 878.5000
- Review Panel
- SU
- Submission Type
- 510(k)