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

Cerafix Dura Substitute

K Number: K153613 · Decision Mar 16, 2016
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
42
Applicant Total
7
Review Days
90

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Basic Information

Device Name
Cerafix Dura Substitute
K Number
K153613
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5910
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Acera Surgical, Inc.
Date Received
December 17, 2015
Decision Date
March 16, 2016
Product Code
GXQ
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
GXQ Dura Substitute

Similar 510(k) Clearances

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Other Clearances by Acera Surgical, Inc.

K Number Device Name
K251224 Restrata Soft Tissue Reinforcement (STR)
K223725 Restrata® MiniMatrix
K193583 Restrata®
K172603 Cerafix Dura Substitute
K170300 Restrata Wound Matrix
K161278 Cerafix Dura Substitute