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

ATLAS WOUND MATRIX

K Number: K090954 · Decision Jul 30, 2009
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
302
Review Days
115

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
ATLAS WOUND MATRIX
K Number
K090954
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wrightmedicaltechnologyinc
Date Received
April 6, 2009
Decision Date
July 30, 2009
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 Wrightmedicaltechnologyinc

K Number Device Name
K222835 Prophecy Preoperative Navigation Alignment System
K213342 PRO-DENSE LoVisc Bone Graft Substitute
K212996 Sterile PHALINX Hammertoe System
K202815 PROPHECY Preoperative Navigation Alignment System
K201259 ORTHOLOC 2 with 3Di Technology Pilon Fracture Plating System
K200507 PRO-DENSE LoVisc Bone Graft Substitute
K193067 The INBONE™ Total Ankle System, the INFINITY™ Total Ankle System and the INVISION™ Total Ankle Revision System
K191393 INFINITY Total Ankle System, INBONE Total Ankle System
K190970 PROSTEP™ TBI™ (Tailors Bunion Implant) System
K183620 PROSTEP TBC Implant System
Search all 302 clearances from Wrightmedicaltechnologyinc →