510(k) K213573
K213573 is an FDA 510(k) premarket notification submitted by Gunze Limited for the device "PELNAC Wound Matrix". The FDA issued a decision of Substantially Equivalent on February 9, 2022. The device falls under product code KGN (Wound Dressing With Animal-Derived Material(S)), a Class U device. Gunze Limited has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 9, 2022
- Date Received
- November 10, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wound Dressing With Animal-Derived Material(S)
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type