Last synced on 14 November 2025 at 11:06 pm

INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)

Page Type
Cleared 510(K)
510(k) Number
K081194
510(k) Type
Special
Applicant
RSB SPINE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2008
Days to Decision
31 days
Submission Type
Summary

INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)

Page Type
Cleared 510(K)
510(k) Number
K081194
510(k) Type
Special
Applicant
RSB SPINE LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/29/2008
Days to Decision
31 days
Submission Type
Summary