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

MOBILIMB-CPM UPPER/LOWER LIMB DEVICE

K Number: K823495 · Decision Jan 21, 1983
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
402
Review Days
59

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Basic Information

Device Name
MOBILIMB-CPM UPPER/LOWER LIMB DEVICE
K Number
K823495
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Synthes (Usa)
Date Received
November 23, 1982
Decision Date
January 21, 1983
Product Code
BXB
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
BXB Exerciser, Powered

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Other Clearances by Synthes (Usa)

K Number Device Name
K131984 SYNTHES SYNSONIC ULNA NAIL
K111667 SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
K111540 SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
K110789 SYNTHES STERNAL ZIPFIX SYSTEM
K103002 SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM
K103243 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM
K102656 SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K093299 SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM
K102694 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K100776 SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
Search all 402 clearances from Synthes (Usa) →