Last synced on 25 January 2026 at 3:41 am

DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981881
510(k) Type
Traditional
Applicant
Doctor'S Research Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1998
Days to Decision
188 days
Submission Type
Statement

DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981881
510(k) Type
Traditional
Applicant
Doctor'S Research Group, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1998
Days to Decision
188 days
Submission Type
Statement