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

CORTICAL BONE SCREW (EUROPEAN STYLE)

K Number: K905357 · Decision Jan 4, 1991
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
1040
Applicant Total
23
Review Days
37

Basic Information

Device Name
CORTICAL BONE SCREW (EUROPEAN STYLE)
K Number
K905357
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
O'TEC CORP.
Date Received
November 28, 1990
Decision Date
January 4, 1991
Product Code
HWC
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
HWC Screw, Fixation, Bone

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Other Clearances by O'TEC CORP.

K Number Device Name
K943293 SCC22/ SCC26 SHOWER COMMODE CHAIR
K910093 FUTURA FEMORAL HIP STEM
K905347 HAGIE PIN
K905355 BROAD SELF-COMPRESSING PLATE
K905358 CANCELLOUS SCREW
K905333 U.S. TYPE CRUCIATE SLOT BONE SCREW
K905363 FIXATION STAPLE
K905341 RUSH PIN
K905344 KNOWLES PIN
K905342 LAG SCREW
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