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

OneFix Biocomposite Anchors, OneFix Biocomposite Small Anchors, OneFix All Suture Anchors, OneFix Interference Screws, OneFix Cannula System

K Number: K212912 · Decision Nov 4, 2021
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
12
Review Days
52

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Basic Information

Device Name
OneFix Biocomposite Anchors, OneFix Biocomposite Small Anchors, OneFix All Suture Anchors, OneFix Interference Screws, OneFix Cannula System
K Number
K212912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
B-One Ortho, Corp.
Date Received
September 13, 2021
Decision Date
November 4, 2021
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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Other Clearances by B-One Ortho, Corp.

K Number Device Name
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K213673 b-ONE MOBIO Total Knee System
K210483 MOBIO Total Knee System
K202768 KOSMO Femoral Stem
K202429 Mobio Total Knee System
K182705 Juveno Hip System Femoral Stem, b-ONE Primary Acetabular System Cups
K183025 MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component
K180446 b-ONE Total Knee System
Search all 12 clearances from B-One Ortho, Corp. →