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AESCULAP PEEK INTERVERTEBRAL BODY FUSION SYSTEM: A SPACE, CESPACE, PROSPACE, T-SPACE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071983
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2008
Days to Decision
287 days
Submission Type
Summary

AESCULAP PEEK INTERVERTEBRAL BODY FUSION SYSTEM: A SPACE, CESPACE, PROSPACE, T-SPACE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071983
510(k) Type
Traditional
Applicant
AESCULAP IMPLANT SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2008
Days to Decision
287 days
Submission Type
Summary