FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTERMEDICS ORTHOPEDICS SAW BLADE

K Number: K931210 · Decision Nov 18, 1993
Classifications
1
FEI Numbers
304
Registration Numbers
304
Same Product Code
26
Applicant Total
108
Review Days
253

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Basic Information

Device Name
INTERMEDICS ORTHOPEDICS SAW BLADE
K Number
K931210
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4820
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intermedics Orthopedics
Date Received
March 10, 1993
Decision Date
November 18, 1993
Product Code
GFA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GFA Blade, Saw, General & Plastic Surgery, Surgical

Similar 510(k) Clearances

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Other Clearances by Intermedics Orthopedics

K Number Device Name
K970300 NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI
K970498 NATURAL-KNEE II REVISION FEMORAL SPACER LUGS
K970166 NATURAL-HIP SYSTEM COCR REVISION STEM
K970567 SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS
K964357 NATURAL-HIP SYSTEM COCR STEM
K964350 MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA
K962190 PATELLOFEMORAL JOINT PROSTHESIS
K963266 NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED
K963155 INTERMOORE FRACTURE HIP STEM (MODIFY)
K962315 SELECT SHOULDER COCR HUMERAL STEM COMPONENT
Search all 108 clearances from Intermedics Orthopedics →