Cleared Traditional

Kerecis Parvus (50207)

K241080 · Kerecis Limited · General & Plastic Surgery
Aug 2024
Decision
124d
Days
Risk

About This 510(k) Submission

K241080 is an FDA 510(k) clearance for the Kerecis Parvus (50207), a Wound Dressing With Animal-derived Material(s), submitted by Kerecis Limited (Isafjordur, IS). The FDA issued a Cleared decision on August 21, 2024, 124 days after receiving the submission on April 19, 2024. This device falls under the General & Plastic Surgery review panel.

Submission Details

510(k) Number K241080 FDA.gov
FDA Decision Cleared SESE
Date Received April 19, 2024
Decision Date August 21, 2024
Days to Decision 124 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code KGN — Wound Dressing With Animal-derived Material(s)
Device Class