FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇸 Iceland

Kerecis Reconstruct

K Number: K202430 · Decision May 2, 2021
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
4
Applicant Total
10
Review Days
250

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Basic Information

Device Name
Kerecis Reconstruct
K Number
K202430
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Kerecis Limited
Date Received
August 25, 2020
Decision Date
May 2, 2021
Product Code
OXH
Advisory Committee
General, Plastic Surgery
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
OXH Mesh, Surgical, Collagen, Plastic And Reconstructive Surgery

Similar 510(k) Clearances

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

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Other Clearances by Kerecis Limited

K Number Device Name
K251845 Marigen Wound Extra; Kerecis Silicone; Kerecis Parvus
K251844 Kerecis SurgiBind (50241)
K243843 Tendon Protect (50242)
K241080 Kerecis Parvus (50207)
K213231 Kerecis Silicone
K192612 Kerecis Gingiva Graft
K190528 MariGen Wound Extra
K153364 Kerecis SecureMesh
K132343 MARIGEN WOUND DRESSING