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MODULOCK POSTERIOR SPINAL FIXATION

Page Type
Cleared 510(K)
510(k) Number
K902397
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/5/1990
Days to Decision
159 days

MODULOCK POSTERIOR SPINAL FIXATION

Page Type
Cleared 510(K)
510(k) Number
K902397
510(k) Type
Traditional
Applicant
ZIMMER, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/5/1990
Days to Decision
159 days