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

LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS

K Number: K113559 · Decision Dec 29, 2011
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
10
Review Days
28

Basic Information

Device Name
LDR SPINE CERVICAL INTERBODY FUSION SYSTME-ROI-C LORDOTIC IMPLANTS
K Number
K113559
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ldr Spine USA, Inc.
Date Received
December 1, 2011
Decision Date
December 29, 2011
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 Ldr Spine USA, Inc.

K Number Device Name
K162133 VerteFIT Corpectomy Cage System
K161173 Avenue® T TLIF Cage
K161798 FacetBRIDGE® System
K142645 Avenue T TLIF Cage
K133363 INTERBRIDGE INTERSPINOUS POSTERIOR FIXATION SYSTEM
K123134 EASYSPINE SYSTEM
K121103 LDR SPINE USA SPINE TUNE, TL SPINAL SYSTEM, LDR SPINE USA EASYSPINE, POSTERIOR SPINAL SYSTEM, LDR SPINE USA MC IMPLANT S
K113285 LDR SPINE USA AVENUE L INTERBODY FUSION
K120760 LDR SPINE SPINETUNE TL SPINAL SYSTEM