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

AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHOR

K Number: K070773 · Decision Oct 11, 2007
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
19
Review Days
204

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Basic Information

Device Name
AXYA, MODEL 3000 AXYZLOOP TITANIUM BONE ANCHOR
K Number
K070773
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Axya Medical, Inc.
Date Received
March 21, 2007
Decision Date
October 11, 2007
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

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Other Clearances by Axya Medical, Inc.

K Number Device Name
K070253 AXYA SUTURE WELDING SYSTEM AND KIT
K063194 TUFFLEX POLYESTER SUTURE
K060165 AXYAFLEX POLYESTER SUTURE
K060970 AXYALOOP NONABSORBABLE BONE ANCHOR
K052491 AXYA MODEL 6500 AXYALOOP SELF-TAPPING BONE ANCHOR
K051983 MODEL 3000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K051250 AXYA, MODEL 6500 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K041698 AXYA MEDICAL, INC. MODEL 5000 AXYALOOP BIO-ABSORBABLE BONE ANCHOR
K022207 AXYA MODEL 3000 AXYALOOP TITANIUM BONE ANCHOR SYSTEM
K021929 AXYA MEDICAL, INC, MODEL 100 SONIC SCALPEL ULTRASONIC SURGICAL SYSTEM
Search all 19 clearances from Axya Medical, Inc. →