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Peridot-TD Spacer system (The Peridot-TD Intervertebral body fusion system); Anterior cervical interbody fusion-ACIF (The Peridot-TD Anterior Cervical Intervertebral body fusion system)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230708
510(k) Type
Traditional
Applicant
GBS Commonwealth Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/22/2023
Days to Decision
69 days
Submission Type
Summary

Peridot-TD Spacer system (The Peridot-TD Intervertebral body fusion system); Anterior cervical interbody fusion-ACIF (The Peridot-TD Anterior Cervical Intervertebral body fusion system)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230708
510(k) Type
Traditional
Applicant
GBS Commonwealth Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
5/22/2023
Days to Decision
69 days
Submission Type
Summary