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

OrthoButton AL

K Number: K230212 · Decision Feb 23, 2023
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
11
Review Days
28

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Basic Information

Device Name
OrthoButton AL
K Number
K230212
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Riverpoint Medical, LLC
Date Received
January 26, 2023
Decision Date
February 23, 2023
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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Other Clearances by Riverpoint Medical, LLC

K Number Device Name
K253693 Strut Suture; No-Tie Button
K253695 LigaMend
K243988 RootMend MRR
K242494 OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct
K232411 JuggerKnot Soft Anchor OC
K231078 All-Suture Anchor
K231278 Knotless Suture Anchor
K220765 HS Fiber Cerclage
K231128 JuggerKnot Soft Anchor
K202242 HS Fiber
Search all 11 clearances from Riverpoint Medical, LLC →