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

Fixone Biocomposite Interference Screw

K Number: K193497 · Decision Jan 5, 2021
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
10
Review Days
385

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Basic Information

Device Name
Fixone Biocomposite Interference Screw
K Number
K193497
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
December 17, 2019
Decision Date
January 5, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), 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
K192709 Fixone All Suture Anchor
K192484 Fixone Biocomposite Anchor
K192032 Fixone Biocomposite Small Anchor
K171299 Fixone Biocomposite Anchor
K162070 JOINIX CANNULAR SYSTEM