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

iovera system

K Number: K173763 · Decision Feb 28, 2018
Classifications
1
FEI Numbers
10
Registration Numbers
10
Same Product Code
22
Applicant Total
9
Review Days
79

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Basic Information

Device Name
iovera system
K Number
K173763
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4250
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Myoscience, Inc.
Date Received
December 11, 2017
Decision Date
February 28, 2018
Product Code
GXH
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GXH Device, Surgical, Cryogenic

Similar 510(k) Clearances

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

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Other Clearances by Myoscience, Inc.

K Number Device Name
K161835 iovera system
K142866 Myoscience iovera system
K133453 IOVERA
K123516 CRYO-TOUCH IV
K120415 CRYO-TOUCH III
K102021 CRYO-TOUCH II
K100447 MYOSCIENCE CRYO-TOUCH
K083493 MYOSCIENCE CRYO-TOUCH