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CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963899
510(k) Type
Traditional
Applicant
EXMOOR PLASTICS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/22/1997
Days to Decision
329 days
Submission Type
Statement

CAUSSE UNIVERSAL OSSICULAR REPLACEMENT PROSTHESIS (ORP/1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963899
510(k) Type
Traditional
Applicant
EXMOOR PLASTICS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
8/22/1997
Days to Decision
329 days
Submission Type
Statement