FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

VersaWrap Tendon Protector

K Number: K160364 · Decision Jun 10, 2016
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
9
Applicant Total
7
Review Days
122

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Basic Information

Device Name
VersaWrap Tendon Protector
K Number
K160364
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
Alafair Biosciences, Inc.
Date Received
February 9, 2016
Decision Date
June 10, 2016
Product Code
OWW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
OWW Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon

Similar 510(k) Clearances

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

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Other Clearances by Alafair Biosciences, Inc.

K Number Device Name
K240817 VersaWrap
K232029 VersaWrap Nerve Protector
K213163 VersaWrap
K203600 VersaWrap
K201631 VersaWrap Nerve Protector
K200311 VersaWrap Tendon Protector