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OREGON FIXATION SYSTEM INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K932027
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/23/1994
Days to Decision
303 days
Submission Type
Summary

OREGON FIXATION SYSTEM INTERFERENCE SCREW

Page Type
Cleared 510(K)
510(k) Number
K932027
510(k) Type
Traditional
Applicant
ACUMED, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
2/23/1994
Days to Decision
303 days
Submission Type
Summary