FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

OSSIOfiber® Suture Anchor

K Number: K254055 · Decision Feb 24, 2026
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
20
Review Days
69

Basic Information

Device Name
OSSIOfiber® Suture Anchor
K Number
K254055
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OSSIO , Ltd.
Date Received
December 17, 2025
Decision Date
February 24, 2026
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 OSSIO , Ltd.

K Number Device Name
K254077 OSSIOfiber® Threaded Trimmable Fixation Nail
K252022 OSSIOfiber® Interference Screw
K251309 OSSIOfiber® Suture Anchor
K243760 OSSIOfiber® Suture Anchor 2.5-3.5 mm
K241932 OSSIOfiber® Compression Staple
K241277 OSSIOfiber® Threaded Trimmable Fixation Nail
K233198 OSSIOfiber® Threaded Trimmable Fixation Nails
K231272 OSSIOfiber® Pin Product Family, OSSIOfiber® Compression Screw, OSSIOfiber® Trimmable Fixation Nail
K233302 OSSIOfiber® Compression Staple
K230750 OSSIOfiber® Cannulated Trimmable Fixation Nail
Search all 20 clearances from OSSIO , Ltd. →