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

INEX Absorbable Nasal Implant

K Number: K152958 · Decision Dec 4, 2015
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
14
Applicant Total
3
Review Days
58

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Basic Information

Device Name
INEX Absorbable Nasal Implant
K Number
K152958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3620
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spirox, Inc.
Date Received
October 7, 2015
Decision Date
December 4, 2015
Product Code
NHB
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
NHB Polymer, Ear, Nose And Throat, Synthetic, Absorbable

Similar 510(k) Clearances

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

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Other Clearances by Spirox, Inc.

K Number Device Name
K161191 Latera Absorbable Nasal Implant
K132920 SPIROX INEX DEVICE