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

Stryker Universal Mesh

K Number: K170773 · Decision Nov 8, 2017
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
291
Applicant Total
92
Review Days
239

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Basic Information

Device Name
Stryker Universal Mesh
K Number
K170773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4760
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker
Date Received
March 14, 2017
Decision Date
November 8, 2017
Product Code
JEY
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
JEY Plate, Bone

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