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

TITANIUM SUTURE ANCHOR

K Number: K133229 · Decision Jan 30, 2014
Classifications
1
FEI Numbers
263
Registration Numbers
263
Same Product Code
564
Applicant Total
4
Review Days
101

Basic Information

Device Name
TITANIUM SUTURE ANCHOR
K Number
K133229
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MTP SOLUTIONS LLC
Date Received
October 21, 2013
Decision Date
January 30, 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

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