Atlas FDA

MEC HIP BOLT

FDA 510(k) clearance K850413 · decided 1985-07-15

Clearance details

K-number
K850413
Device name
MEC HIP BOLT
Applicant
Pfizer, Inc.
Decision
Substantially Equivalent
Date received
1985-02-04
Decision date
1985-07-15
Days to decision
161 days
Clearance type
Traditional
Product code
KTT
Device class
2
Regulation number
888.3030
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
Ny, NY, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

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Medusa Orthopedics Boa External Fixation System (K252555)Medusa Orthopedics, LLC2025-11-25
The Response Ortho Smart Fixator - Hexapod System (K252625)Response Ortho Solutions, LLC2025-11-20
External Fixation Mini Rail System (K252106)Paragon 28, Inc.2025-09-30
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
GELFOAM (absorbable gelatin gel, powder from abs. gel, sponge USP), GELFOAM (compressed absorbable gelatin sponge, USP), (N18286/S041)Pfizer, Inc.2023-05-16
(Gelfoam (absorbable gelatin) Sterile Sponge) (N18286/S040)Pfizer, Inc.2022-06-24
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S039)Pfizer, Inc.2021-07-08
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S038)Pfizer, Inc.2021-05-07
Gelfoam Sterile Sponge (N18286/S037)Pfizer, Inc.2021-02-24
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S036)Pfizer, Inc.2020-12-10
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S035)Pfizer, Inc.2020-03-19
Gelfoam (absorbable gelatin) Sterile Sponge (N18286/S034)Pfizer, Inc.2020-02-27