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

SECURE Screw

K Number: K191771 · Decision Oct 16, 2019
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
6
Review Days
106

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Basic Information

Device Name
SECURE Screw
K Number
K191771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
A.M. Surgical, Inc.
Date Received
July 2, 2019
Decision Date
October 16, 2019
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

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K Number Device Name
K191345 Pegasus System
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K042458 A.M. SURGICAL CPF DISTAL RADIAL EXTERNAL CROSS PIN FIXATION SYSTEM
K982142 MOUNTABLE ENDOSCOPIC KNIFE