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

restor3d Pin Implants

K Number: K211789 · Decision Jan 4, 2022
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
12
Review Days
208

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
restor3d Pin Implants
K Number
K211789
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Restor3D
Date Received
June 10, 2021
Decision Date
January 4, 2022
Product Code
HTY
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
HTY Pin, Fixation, Smooth

Similar 510(k) Clearances

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

View all

Other Clearances by Restor3D

K Number Device Name
K253992 Veritas Reverse Total Shoulder System
K252454 Kinos Total Ankle System
K243643 restor3d Reverse Total Shoulder Arthroplasty System
K242868 Kinos Total Ankle System
K241482 Kinos Total Ankle System
K234087 restor3d TIDAL Lumbar Interbody Fusion System
K232595 Kinos Axiom Total Ankle System
K231458 Extremity Staple
K223326 Axiom PSR System
K220523 restor3d TiDAL Lumbar Interbody Fusion Device
Search all 12 clearances from Restor3D →