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

Aevumed PHANTOM Suture Anchors

K Number: K242895 · Decision Aug 6, 2025
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
7
Review Days
317

Basic Information

Device Name
Aevumed PHANTOM Suture Anchors
K Number
K242895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Aevumed, Inc.
Date Received
September 23, 2024
Decision Date
August 6, 2025
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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K222363 Aevumed PHANTOM™-LP Suture Anchors
K180464 AEVUMED PHANTOM Suture Anchors