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ARTHROPLANE

Page Type
Cleared 510(K)
510(k) Number
K932869
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1994
Days to Decision
284 days
Submission Type
Summary

ARTHROPLANE

Page Type
Cleared 510(K)
510(k) Number
K932869
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/25/1994
Days to Decision
284 days
Submission Type
Summary