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

PuraPly Micronized Wound Matrix (PuraPly MZ)

K Number: K220317 · Decision Jul 1, 2022
Classifications
1
FEI Numbers
134
Registration Numbers
134
Same Product Code
187
Applicant Total
12
Review Days
148

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Basic Information

Device Name
PuraPly Micronized Wound Matrix (PuraPly MZ)
K Number
K220317
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Organogenesis, Inc.
Date Received
February 3, 2022
Decision Date
July 1, 2022
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.

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Other Clearances by Organogenesis, Inc.

K Number Device Name
K212579 FortiShield (Biosynthetic Wound Matrix)
K071555 FORTAGEN ORAL MEMBRANE
K051647 FORTADERM ANTIMICROBIAL WOUND DRESSING
K042809 CUFFPATCH
K021107 FORTAFLEX SURGICAL SLING
K021105 FORTAFLEX SURGICAL MESH
K020049 FORTAFLEX SURGICAL MESH
K011025 FORTAFLEX SURGICAL MESH
K011026 FORTADERM WOUND DRESSING
K011027 FORTAFLEX SURGICAL SLING
Search all 12 clearances from Organogenesis, Inc. →