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PIONEER LABORATORIES BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940690
510(k) Type
Traditional
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/22/1994
Days to Decision
279 days
Submission Type
Statement

PIONEER LABORATORIES BONE SCREW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K940690
510(k) Type
Traditional
Applicant
PIONEER SURGICAL TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/22/1994
Days to Decision
279 days
Submission Type
Statement