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

OSSIOfiber® Compression Staple

K Number: K241932 · Decision Aug 28, 2024
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
3
Applicant Total
20
Review Days
58

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Basic Information

Device Name
OSSIOfiber® Compression Staple
K Number
K241932
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
July 1, 2024
Decision Date
August 28, 2024
Product Code
MNU
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
MNU Staple, Absorbable

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MNU), 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
K251309 OSSIOfiber® Suture Anchor
K243760 OSSIOfiber® Suture Anchor 2.5-3.5 mm
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. →