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

CAMBER SPINE COVERIS CERVICAL CAGE

K Number: K133529 · Decision Mar 20, 2014
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
4
Review Days
125

Basic Information

Device Name
CAMBER SPINE COVERIS CERVICAL CAGE
K Number
K133529
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Camber Spine
Date Received
November 15, 2013
Decision Date
March 20, 2014
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

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Other Clearances by Camber Spine

K Number Device Name
K143490 VERTA Corpectomy Cage
K133366 ORTHROS POSTERIOR STABILIZATION SYSTEM
K134038 CAMBER SPINE DIAGON OBLIQUE CAGE