Last synced on 14 November 2025 at 11:06 pm

PRIMADO SURGICAL DRILL

Page Type
Cleared 510(K)
510(k) Number
K080722
510(k) Type
Traditional
Applicant
NAKANISHI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2008
Days to Decision
188 days
Submission Type
Statement

PRIMADO SURGICAL DRILL

Page Type
Cleared 510(K)
510(k) Number
K080722
510(k) Type
Traditional
Applicant
NAKANISHI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/2008
Days to Decision
188 days
Submission Type
Statement