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ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001044
510(k) Type
Traditional
Applicant
ACME SPINE, LLC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/3/2000
Days to Decision
217 days

ACME SPINE SYSTEM - SERIES 6000, 7000, MONOAXIAL AND POLYAXIAL SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K001044
510(k) Type
Traditional
Applicant
ACME SPINE, LLC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/3/2000
Days to Decision
217 days