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P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG

Page Type
Cleared 510(K)
510(k) Number
K863854
510(k) Type
Traditional
Applicant
PRECISION MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1986
Days to Decision
48 days

P.M.D. INTRAMEDULLARY CEMENT RESTRICTOR PLUG

Page Type
Cleared 510(K)
510(k) Number
K863854
510(k) Type
Traditional
Applicant
PRECISION MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1986
Days to Decision
48 days