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

C-SPLINT

K Number: K802104 · Decision Sep 16, 1980
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
39
Review Days
13

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Basic Information

Device Name
C-SPLINT
K Number
K802104
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Cutter Laboratories, Inc.
Date Received
September 3, 1980
Decision Date
September 16, 1980
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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Other Clearances by Cutter Laboratories, Inc.

K Number Device Name
K861315 HYPERBARIC PENETRATION EXTENSION SET
K854106 BAYSILEX
K842324 PERFOURM
K834106 INTRAVENOUS INFUSION CONTROLLER
K832237 ORTHOPEDIC CASTING TAPE MAXCAST
K823214 DOSIMETRIC RELEASE PROGRAM - ADMIN. SET
K821326 CUTTER BOND POLYCARBOXYLATE CEMENT
K813532 CUTTERBOND ZINC PHOSPHATE CEMENT
K802105 C-BLADE
K801652 TOTAL PARENTERAL NUTRITION SET BAG
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