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

SEASPINE SPACER SYSTEM

K Number: K102026 · Decision May 12, 2011
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
27
Review Days
297

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
SEASPINE SPACER SYSTEM
K Number
K102026
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Seaspine, Inc.
Date Received
July 19, 2010
Decision Date
May 12, 2011
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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

View all

Other Clearances by Seaspine, Inc.

K Number Device Name
K231654 NorthStar OCT System
K150469 Integra Laminoplasty System
K142488 SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu aPOD-L NanoMetalene, Vu ePOD NanoMetalene
K133418 INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM
K132859 INTEGRA FACET FIXATION SYSTEM
K121924 INTEGRA INTERSPINOUS PROCESS SYSTEM
K130830 INTEGRA LAMINOPLASTY SYSTEM
K122571 MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM
K112206 CARDIFF ANTERIOR CERVICAL PLATE SYSTEM
K111671 SEASPINE MONOPOLAR PROBE SYSYEM
Search all 27 clearances from Seaspine, Inc. →