FDA 510(k), K931588, SUTTER PROXIMAL INTERPHALANGEAL JOINT
FDA 510(k), K931588, SUTTER PROXIMAL INTERPHALANGEAL JOINT
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510(K) Number: K931588
Device Name: SUTTER PROXIMAL INTERPHALANGEAL JOINT
Manufacturer:
Device Classification Name: Prosthesis, Finger, Constrained, Polymer
Regulation Number: 888.3230
Classification Product Code: KYJ
Date Received: 03/31/1993
Decision Date: 03/10/1994
Regulation Medical Specialty: Orthopedic
Device Name: SUTTER PROXIMAL INTERPHALANGEAL JOINT
Manufacturer:
Device Classification Name: Prosthesis, Finger, Constrained, Polymer
Regulation Number: 888.3230
Classification Product Code: KYJ
Date Received: 03/31/1993
Decision Date: 03/10/1994
Regulation Medical Specialty: Orthopedic