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

Matrix HA Fusion Porous Cervical IBF System

K Number: K223510 · Decision Dec 12, 2022
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
33
Review Days
20

Basic Information

Device Name
Matrix HA Fusion Porous Cervical IBF System
K Number
K223510
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovasis, Inc.
Date Received
November 22, 2022
Decision Date
December 12, 2022
Product Code
ODP
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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

Similar 510(k) Clearances

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

View all

Other Clearances by Innovasis, Inc.

K Number Device Name
K251073 Innovasis Navigation Instruments (Vector G-E Navigation Instruments and the Excella G-E Navigation Instruments)
K250182 Innovasis Navigation Instruments
K241276 Vector™ Pedicle Screw System
K231899 HAtetracell™-C Titanium Cervical IBF System
K223511 Excella Navigation Instruments
K220875 HAcancellous PEEK-C Porous HA PEEK Cervical IBF System
K212967 AxTiHA Stand-Alone ALIF System
K201614 TxTiHA IBF System, AxTiHA Stand-Alone ALIF System
K200874 TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End
K192049 Oryx Cervical Plate System
Search all 33 clearances from Innovasis, Inc. →