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

OTI ORTHOPEDIC FASTENER SYSTEM

K Number: K925301 · Decision Mar 16, 1993
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
18
Review Days
146

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Basic Information

Device Name
OTI ORTHOPEDIC FASTENER SYSTEM
K Number
K925301
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Osteo Technology, Inc.
Date Received
October 21, 1992
Decision Date
March 16, 1993
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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Other Clearances by Osteo Technology, Inc.

K Number Device Name
K926156 REPLICA(TM) TOTAL HIP SYSTEM
K922859 ANATOMICAL TYPE KNEE SYSTEM
K922869 TOTAL CONDYLAT TYPE KNEE SYSTEM
K925447 OTI ORTHOPEDIC WIRE SYSTEM
K926213 MODIFIED ZICKEL INTRAMEDULLARY ROD SYSTEM
K922861 BIOMETRIC SCREW FIXATION CUP
K922870 THREE SPIKE CUP
K922682 AMERICANA HIP PROTHESIS
K922871 UNIFIT FEMORAL STEM
K922868 THOMPSON TYPE HIP PROTHESIS
Search all 18 clearances from Osteo Technology, Inc. →