Atlas FDA

SUTTER PROXIMAL INTERPHALANGEAL JOINT

FDA 510(k) clearance K931588 · decided 1994-03-10

Clearance details

K-number
K931588
Device name
SUTTER PROXIMAL INTERPHALANGEAL JOINT
Applicant
Sutter Corp.
Decision
Substantially Equivalent
Date received
1993-03-31
Decision date
1994-03-10
Days to decision
344 days
Clearance type
Traditional
Product code
KYJ
Device class
2
Regulation number
888.3230
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
San Diego, CA, US
Third-party review
No
Expedited review
No

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DEPUY NEUFLEX PIP FINGER (K001922)Depuy, Inc.2000-08-29
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SUTTER FINGER JOINT PROSTHESIS (K870200)Sutter Biomedical, Inc.1987-10-09
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Recalls involving this device

No recalls on record reference this clearance.