FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Fixone All Suture Anchor

K Number: K192709 · Decision Dec 15, 2020
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
10
Review Days
445

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Basic Information

Device Name
Fixone All Suture Anchor
K Number
K192709
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aju Pharm Co., Ltd.
Date Received
September 27, 2019
Decision Date
December 15, 2020
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 Aju Pharm Co., Ltd.

K Number Device Name
K233601 Fixone Meniscal Repair
K230892 Fixone Biocomposite Anchor
K222423 Fixone All Suture Anchor
K203523 Fixone hybrid knotless anchor
K193497 Fixone Biocomposite Interference Screw
K192484 Fixone Biocomposite Anchor
K192032 Fixone Biocomposite Small Anchor
K171299 Fixone Biocomposite Anchor
K162070 JOINIX CANNULAR SYSTEM