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

Cannulated Fasteners and Nuts

K Number: K211290 · Decision Aug 3, 2021
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
97

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Basic Information

Device Name
Cannulated Fasteners and Nuts
K Number
K211290
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OsteoCentric Technologies
Date Received
April 28, 2021
Decision Date
August 3, 2021
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
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K230242 OsteoCentric Dental Implant System
K230226 Integrity-SI® Fusion System
K230595 OsteoCentric ACL Fixation System
K230764 OsteoCentric Integrated Hip Fastener System
K222512 Integrity-SI Fusion System
K221332 OsteoCentric Spine MIS Pedicle Fastener System
K210754 Cannulated Fasteners and Nuts
Search all 11 clearances from OsteoCentric Technologies →