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

ORTHOSISES DEVICES

K Number: K780225 · Decision Feb 24, 1978
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
441
Review Days
15

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Basic Information

Device Name
ORTHOSISES DEVICES
K Number
K780225
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Biomet, Inc.
Date Received
February 9, 1978
Decision Date
February 24, 1978
Product Code
IQI
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
IQI Orthosis, Limb Brace

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K221968 StageOne™ Shoulder Cement Spacer Molds
K213287 StageOne Knee Cement Spacer Molds
K212431 Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve
K212435 Comprehensive Humeral Fracture Positioning Sleeves
K210192 A.L.P.S. Clavicle Plating System
K193214 WasherLoc and No-Profile Screw and Washer Systems, Biomet Cannulated Screw System, Biomet Headless Compression and Twist-Off Screws
K193546 Distal Centralizers
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