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

CAMBRIA

K Number: K082309 · Decision Apr 9, 2009
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
27
Review Days
239

Basic Information

Device Name
CAMBRIA
K Number
K082309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Seaspine, Inc.
Date Received
August 13, 2008
Decision Date
April 9, 2009
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 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. →