FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇷 Brazil

Cannulated Screws Neoortho

K Number: K162874 · Decision Jun 27, 2017
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
5
Review Days
257

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Basic Information

Device Name
Cannulated Screws Neoortho
K Number
K162874
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Neoortho Produtos Ortopedicos S/A
Date Received
October 13, 2016
Decision Date
June 27, 2017
Product Code
HWC
Advisory Committee
Orthopedic
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

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

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Other Clearances by Neoortho Produtos Ortopedicos S/A

K Number Device Name
K141103 INTRAMEDULLARY NAIL AND SCREWS-NEONAIL
K132852 PEEK CAGE FOR THE VERTEBRAL SPINE
K113733 SMALL AND LARGE FRAGMENTS OSTEOSYNTHESIS SYSTEM NEOFIX
K102641 MINI AND MICRO FRAGMENTS RECONSTRUCTION SYSTEM-NEOFACE