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

OSSIOfiber® Threaded Trimmable Fixation Nails

K Number: K233198 · Decision Mar 8, 2024
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
20
Review Days
162

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
OSSIOfiber® Threaded Trimmable Fixation Nails
K Number
K233198
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OSSIO , Ltd.
Date Received
September 28, 2023
Decision Date
March 8, 2024
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

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

View all

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
K241932 OSSIOfiber® Compression Staple
K241277 OSSIOfiber® Threaded Trimmable Fixation Nail
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. →