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MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884888
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/29/1988
Days to Decision
37 days

MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884888
510(k) Type
Traditional
Applicant
PROTEK, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/29/1988
Days to Decision
37 days