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GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103712
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2011
Days to Decision
81 days
Submission Type
Summary

GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K103712
510(k) Type
Traditional
Applicant
DEPUY MITEK, A JOHNSON & JOHNSON COMPANY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/2011
Days to Decision
81 days
Submission Type
Summary