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

X-POD ADJUSTABLE VERTEBRAL BODY REPLACEMENT

K Number: K070786 · Decision Jun 28, 2007
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
276
Applicant Total
23
Review Days
98

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Basic Information

Device Name
X-POD ADJUSTABLE VERTEBRAL BODY REPLACEMENT
K Number
K070786
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Theken Spine, LLC
Date Received
March 22, 2007
Decision Date
June 28, 2007
Product Code
MQP
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
MQP Spinal Vertebral Body Replacement Device

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Other Clearances by Theken Spine, LLC

K Number Device Name
K121482 INSTRUMENT SYSTEM FOR ENDOSCOPIC SPINAL SURGERY
K121211 VU APOD INTERVERTEBRAL BODY FUSION DEVICE
K120829 STAINLESS STEEL SPINAL SYSTEM
K120047 CORAL SPINAL SYSTEM
K111675 VU C*POD INTERVERTEBRAL BODY FUSION DEVICE
K103228 PARAMOUNT R IBF DEVICE
K102323 CERVICAL STANDALONE INTERVERTEBRAL BODY FUSION DEVICE
K101310 VU APOD INTERVERTEBRAL BODY FUSION DEVICE
K100970 STAINLESS STEEL SPINAL SYSTEM
K091266 THEKEN CORAL SPINAL SYSTEM
Search all 23 clearances from Theken Spine, LLC →