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

ICONIX ALL SUTURE ANCHORS

K Number: K133671 · Decision Feb 28, 2014
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
124
Review Days
91

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
ICONIX ALL SUTURE ANCHORS
K Number
K133671
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
November 29, 2013
Decision Date
February 28, 2014
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.

View all

Other Clearances by Stryker Corp.

K Number Device Name
K230045 HipCheck
K191259 Stryker CrossFlow Integrated Arthroscopy Pump
K182359 HipCheck
K143399 Stryker Footed Attachments and Cutting Accessories
K143320 Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments
K150449 LITe Plate System
K142381 Xia 3 Spinal System
K122113 MEMORY METAL STAPLES, EASYCLIP
K122284 HOFFMANN 3
K122053 SHAPEMATCH CUTTING GUIDE
Search all 124 clearances from Stryker Corp. →