Last synced on 14 June 2024 at 11:05 pm

REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080418
510(k) Type
Traditional
Applicant
REGENERATION TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
75 days
Submission Type
Summary

REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K080418
510(k) Type
Traditional
Applicant
REGENERATION TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2008
Days to Decision
75 days
Submission Type
Summary