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POWERGRIP(TM) COMPRESSION FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K950009
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1995
Days to Decision
227 days
Submission Type
Statement

POWERGRIP(TM) COMPRESSION FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K950009
510(k) Type
Traditional
Applicant
SYNVASIVE TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1995
Days to Decision
227 days
Submission Type
Statement