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

Integrity™ Bone Staple Fixation System

K Number: K223860 · Decision May 22, 2023
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
9
Review Days
150

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Basic Information

Device Name
Integrity™ Bone Staple Fixation System
K Number
K223860
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Anika Therapeutics, Inc.
Date Received
December 23, 2022
Decision Date
May 22, 2023
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

Similar 510(k) Clearances

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

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Other Clearances by Anika Therapeutics, Inc.

K Number Device Name
K250997 Integrity™ Implant
K231968 Tactoset® Injectable Bone Substitute
K223538 Integrity Implant
K222487 Anika Tissue Tack Fixation System
K223915 Tactoset
K212083 Tactoset Injectable Bone Substitute
K190956 SCS 17-01
K173008 SCS 17-01