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TITANIUM GDLH POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954645
510(k) Type
Traditional
Applicant
SOFAMOR DANEK USA,INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/16/1996
Days to Decision
98 days

TITANIUM GDLH POSTERIOR SPINAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954645
510(k) Type
Traditional
Applicant
SOFAMOR DANEK USA,INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
1/16/1996
Days to Decision
98 days