Atlas FDA

MEDICINELODGE ZIPKNOT

FDA 510(k) clearance K051488 · decided 2005-07-27

Clearance details

K-number
K051488
Device name
MEDICINELODGE ZIPKNOT
Applicant
Medicinelodge, Inc.
Decision
Substantially Equivalent
Date received
2005-06-06
Decision date
2005-07-27
Days to decision
51 days
Clearance type
Traditional
Product code
NVH
Device class
2
Regulation number
878.4300
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Logan, UT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.