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PEDIGUARD NERVE DETECTOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123390
510(k) Type
Traditional
Applicant
SPINEGUARD, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2013
Days to Decision
279 days
Submission Type
Statement

PEDIGUARD NERVE DETECTOR SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K123390
510(k) Type
Traditional
Applicant
SPINEGUARD, S.A.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/2013
Days to Decision
279 days
Submission Type
Statement