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

OSSIOfiber® Suture Anchor

K Number: K251309 · Decision May 27, 2025
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
20
Review Days
29

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Basic Information

Device Name
OSSIOfiber® Suture Anchor
K Number
K251309
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OSSIO , Ltd.
Date Received
April 28, 2025
Decision Date
May 27, 2025
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MAI), ordered by most recent decision date.

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Other Clearances by OSSIO , Ltd.

K Number Device Name
K254077 OSSIOfiber® Threaded Trimmable Fixation Nail
K254055 OSSIOfiber® Suture Anchor
K252022 OSSIOfiber® Interference Screw
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. →