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LUQUE SEGMENTAL SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
510(k) Number
K913561
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1992
Days to Decision
160 days
Submission Type
Statement

LUQUE SEGMENTAL SPINAL INSTRUMENTATION

Page Type
Cleared 510(K)
510(k) Number
K913561
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/1992
Days to Decision
160 days
Submission Type
Statement