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

SYNERGY ADJUSTABLE TRANSVERSE CONNECTOR ROD, SYNERGY ADJUSTABLE TRANSVERSE CONNECTOR LAMP

K Number: K000876 · Decision Apr 18, 2000
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
39
Review Days
29

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Basic Information

Device Name
SYNERGY ADJUSTABLE TRANSVERSE CONNECTOR ROD, SYNERGY ADJUSTABLE TRANSVERSE CONNECTOR LAMP
K Number
K000876
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Interpore Cross Intl.
Date Received
March 20, 2000
Decision Date
April 18, 2000
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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Other Clearances by Interpore Cross Intl.

K Number Device Name
K050861 PEEK CAS
K031399 INTERGRO DBM
K041407 TITANIUM MESH IMPLANT
K043229 MODIFICATION TO ALTIUS OCT SYSTEM
K042798 C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM
K040928 EXPANDABLE PEEK VBR IMPLANT
K041794 C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM
K041449 SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SEAT
K033961 ALTIUS OCT SYSTEM
K040168 MODIFICATION TO GEO STRUCTURE
Search all 39 clearances from Interpore Cross Intl. →