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

Seaspine WaveForm C Interbody System

K Number: K201073 · Decision Sep 18, 2020
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
150
Applicant Total
62
Review Days
149

Basic Information

Device Name
Seaspine WaveForm C Interbody System
K Number
K201073
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SeaSpine Orthopedics Corporation
Date Received
April 22, 2020
Decision Date
September 18, 2020
Product Code
OVE
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
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

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Other Clearances by SeaSpine Orthopedics Corporation

K Number Device Name
K250908 Virata Spinal Fixation System
K243659 FLASH™ Facet Fusion Instruments, IsoTis® Facet Fusion Instruments
K242273 Cove Putty, OsteoCove Putty
K241466 Shoreline ACS Interbody System; Shoreline RT Interbody System; Regatta Lateral System; Reef L Interbody System; Reef TO/TA System; Meridian Interbody System; WaveForm C Interbody System; WaveForm L Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; WaveForm A Interbody System
K240566 Reef L Interbody System; WaveForm L Interbody System
K232566 NewPort Spinal System; Daytona Small Stature Spinal System; Malibu Spinal System; Mariner Pedicle Screw Systems: Mariner Outrigger Revision System; Mariner MIS Pedicle Screw System; Mariner Deformity System; Mariner RDX System
K233694 Meridian Interbody System; WaveForm A Interbody System
K233414 Shoreline ACS Interbody System; Shoreline RT Interbody System
K232668 Cove Strip, OsteoCove Strip
K231030 Cove Putty, OsteoCove Putty
Search all 62 clearances from SeaSpine Orthopedics Corporation →