FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

InnovaMatrix FS

K Number: K210580 · Decision Apr 21, 2021
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
4
Review Days
54

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
InnovaMatrix FS
K Number
K210580
Device Class
FDA unclassified
Clearance Type
Special
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Triad Life Sciences, Inc.
Date Received
February 26, 2021
Decision Date
April 21, 2021
Product Code
KGN
Advisory Committee
Unknown
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGN Wound Dressing With Animal-Derived Material(S)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KGN), ordered by most recent decision date.

View all

Other Clearances by Triad Life Sciences, Inc.

K Number Device Name
K213716 InnovaBurn
K211902 InnovaMatrix PD
K193552 InnovaMatrix