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MOBILIMB-CPM UPPER/LOWER LIMB DEVICE

Page Type
Cleared 510(K)
510(k) Number
K823495
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1983
Days to Decision
59 days

MOBILIMB-CPM UPPER/LOWER LIMB DEVICE

Page Type
Cleared 510(K)
510(k) Number
K823495
510(k) Type
Traditional
Applicant
SYNTHES (USA)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/21/1983
Days to Decision
59 days