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ANTERIOR KYPHOSIS DISTRACTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K802222
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1980
Days to Decision
28 days

ANTERIOR KYPHOSIS DISTRACTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K802222
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/1980
Days to Decision
28 days